U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C7H7ClO2S
Molecular Weight 190.647
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of p-Toluenesulfonyl chloride

SMILES

CC1=CC=C(C=C1)S(Cl)(=O)=O

InChI

InChIKey=YYROPELSRYBVMQ-UHFFFAOYSA-N
InChI=1S/C7H7ClO2S/c1-6-2-4-7(5-3-6)11(8,9)10/h2-5H,1H3

HIDE SMILES / InChI
Molecular Formula C7H7ClO2S
Molecular Weight 190.647
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Unknown
149124
PubMed

PubMed

TitleDatePubMed
N-(4-Meth-oxy-phen-yl)-4-methyl-benzene-sulfonamide.
2010-12-18
N-(2,6-Dichloro-phen-yl)-4-methyl-benzene-sulfonamide.
2010-12-15
N-(3,4-Dichloro-phen-yl)-4-methyl-benzene-sulfonamide.
2010-12-11
N-(2,5-Dichloro-phen-yl)-4-methyl-benzene-sulfonamide.
2010-12-04
N-(2,3-Dimethyl-phen-yl)-4-methyl-benzene-sulfonamide.
2010-11-27
N-(4-Chloro-pyridin-2-yl)-N-meth-oxy-methyl-4-methyl-benzene-sulfonamide.
2010-11-27
N-(4-Chloro-pyridin-2-yl)-N-(4-methyl-phenyl-sulfon-yl)acetamide.
2010-11-27
N-(2,3-Dichloro-phen-yl)-4-methyl-benzene-sulfonamide.
2010-11-06
N-(2-Meth-oxy-phen-yl)-4-methyl-benzene-sulfonamide.
2010-10-30
2,2,2-Trifluoro-ethyl 4-methyl-benzene-sulfonate.
2010-10-09
[(3R,4S)-4-(4-Fluoro-phen-yl)-1-methyl-piperidin-3-yl]methyl 4-methyl-benzene-sulfonate.
2010-09-30
Synthesis and crystal structures of multifunctional tosylates as basis for star-shaped poly(2-ethyl-2-oxazoline)s.
2010-09-09
4-Methyl-N-[(E)-4-methyl-1-(4-methyl-phenyl-sulfon-yl)-1,2-dihydropyridin-2-yl-idene]benzene-sulfonamide.
2010-07-03
N-(3-Eth-oxy-phen-yl)-4-methyl-benzene-sulfonamide.
2010-06-16
N-(2,6-Dimethyl-phen-yl)-4-methyl-benzene-sulfonamide.
2010-04-24
3-[1-(4-Methyl-phen-ylsulfon-yl)-1,4-di-hydro-pyridin-4-yl]-1H-indole.
2010-03-24
N-(p-Tolyl-sulfon-yl)-l-asparagine.
2010-02-06
Methyl 2-(p-toluene-sulfonamido)benzoate.
2010-01-13
N-[4-(p-Toluenesulfonamido)phen-ylsulfon-yl]acetamide.
2010-01-09
N-(3-Bromo-5-methyl-2-pyrid-yl)-4-methyl-benzene-sulfonamide.
2009-12-19
N-(3,5-Dimethyl-phen-yl)-4-methyl-benzene-sulfonamide.
2009-12-16
N-(2,5-Dimethyl-phen-yl)-4-methyl-benzene-sulfonamide.
2009-12-04
2-(4-Methyl-benzene-sulfonamido)-2-phenyl-acetic acid.
2009-10-17
4-(9-Anthr-yl)-1-(3-bromo-phen-yl)spiro-[azetidine-3,9'-xanthen]-2-one.
2009-09-26
3,4-O-Isopropyl-idene-2,7-di-O-p-tolyl-sulfonyl-α-l-xylo-3-heptulo-3,6-furan-osononitrile.
2009-09-12
N,N'-Bis(2-cyano-ethyl)-4,4'-dimethyl-N,N'-(butane-1,4-di-yl)dibenzene-sulfonamide.
2009-09-12
2,2,4-Trimethyl-5-(4-tolyl-sulfon-yl)-2,3,4,5-tetra-hydro-1H-1,5-benzo-diazepine.
2009-09-05
N-(3,5-Dichloro-phen-yl)-4-methyl-benzene-sulfonamide.
2009-09-05
4-(4-Cyano-2-fluoro-phen-oxy)phenyl 4-methyl-benzene-sulfonate.
2009-07-29
4-(9-Anthr-yl)-1-(2,4-dimethoxy-phen-yl)spiro-[azetidine-3,9'-xanthen]-2-one.
2009-06-20
(2S)-Methyl 2-(p-toluenesulfonamido)propanoate.
2009-05-14
N-(3,4-Dimethyl-phen-yl)-4-methyl-benzene-sulfonamide.
2009-03-28
4-(9-Anthr-yl)-1-(2-methoxy-phen-yl)spiro-[azetidin-3,9'-xanthen]-2-one.
2009-02-28
4-(9-Anthr-yl)-1-phenylspiro-[azetidine-3,9'-xanthen]-2-one.
2009-02-11
Capture of Escherichia coli O157:H7 Using Immunomagnetic Beads of Different Size and Antibody Conjugating Chemistry.
2009
2,4-Di-tert-butyl-6-[1-(3,5-di-tert-butyl-2-hydroxy-phen-yl)eth-yl]phenyl 4-methyl-benzene-sulfonate.
2008-12-17
1-(Phthalimidometh-yl)pyridinium p-toluene-sulfonate.
2008-12-10
4-(9-Anthr-yl)-1-(1-naphth-yl)spiro-[azetidine-3,9'-xanthen]-2-one n-hexane hemisolvate.
2008-11-29
(1R,3S,5R,6S)-6-Acet-oxy-3-(4-methyl-phenyl-sulfon-yloxy)tropane.
2008-11-13
1,2-Bis(p-tolyl-sulfon-yl)hydrazine.
2008-10-25
6-Formyl-2-meth-oxy-3-nitro-phenyl 4-toluene-sulfonate.
2008-09-30
trans-rac-[1-Oxo-2-phenethyl-3-(2-thien-yl)-1,2,3,4-tetra-hydro-isoquinolin-4-yl]methyl 4-methyl-benzene-sulfonate.
2008-09-17
2-Nitro-p-phenyl-ene bis-(toluene-sulfonate).
2008-08-23
1-(2,3-Di-O-acetyl-4-chloro-4-de-oxy-6-O-tosyl-β-d-galactopyranos-yl)propan-2-one methanol 0.25-solvate.
2008-07-19
Tetra-O-4-methyl-phenyl-sulfonyl-penta-erythritol.
2008-07-12
O-(tert-Butyl-dimethyl-silyl)tris-(O-4-methyl-phenyl-sulfon-yl)penta-erythritol.
2008-07-12
2-[1-(4-Ethoxy-phen-yl)-2-oxo-4-styryl-azetidin-3-yl]isoindoline-1,3-dione.
2008-04-26
4-(9-Anthr-yl)-1-(4-methoxy-phen-yl)spiro-[azetidin-3,9'-xanthen]-2-one.
2008-04-26
4-(Methyl-sulfan-yl)-2-(p-toluene-sulfonamido)butanoic acid.
2008-03-12
1-Isopropyl-4-tosyl-piperazin-1-ium trifluoro-acetate.
2007-12-06
Patents

Patents

03932381
1
03959309
5
03962354
1
03966773
135
03975443
21
03983111
5
04002766
7
04029788
4
04029809
1
04046914
2
04049663
21
04059630
1
04094896
1
04123613
1
04147804
3
04148909
5
04150235
3
04151352
2
04151360
1
04160085
1
04167515
5
04187216
3
04206156
1
JP2001048859A
1
JP2011524942A
3
JPH01144491A
1
JPH01230601A
1
JPH0273067A
1
JPH0425503A
1
JPH04264062A
1
JPH06179682A
1
JPH06247960A
1
JPH07145169A
1
JPH07165743A
1
JPH072741A
1
JPH08325187A
1
JPH09169764A
1
JPH11343300A
1
JPS56142270A
1
JPS562923A
2
JPS5651498A
1
JPS5724377A
1
JPS5750956A
1
JPS58194841A
1
JPS60126279A
1
JPS6048972A
1
JPS61189258A
1
JPS61189264A
1
JPS62198656A
1
JPS6327481A
1
JPS638365A
1
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:13:29 GMT 2025
Edited
by admin
on Mon Mar 31 21:13:29 GMT 2025
Record UNII
027KYN78B4
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
p-Toluenesulfonyl chloride
MI  
Common Name English
NSC-175822
Preferred Name English
P-TOLUENESULFONIC CHLORIDE
Common Name English
4-METHYLBENZENE-1-SULFONYL CHLORIDE
Systematic Name English
4-TOLUOLSULFONYL CHLORIDE
Systematic Name English
4-METHYLPHENYLSULFONYL CHLORIDE
Systematic Name English
P-TOLUENSULFONYL CHLORIDE
Common Name English
P-TOLUENESULFONYL CHLORIDE [MI]
Common Name English
P-TOLUENESULPHONYL CHLORIDE
Common Name English
TOSYL CHLORIDE
Systematic Name English
P-TOSYL CHLORIDE
Common Name English
TOLUENESULFONYL CHLORIDE
Systematic Name English
P-TOLYLSULFONYL CHLORIDE
Common Name English
P-TOLUENESULFONIC ACID CHLORIDE
Common Name English
P-METHYLBENZENESULFONYL CHLORIDE
Common Name English
P-METHYLPHENYLSULFONYL CHLORIDE
Common Name English
4-TOSYL CHLORIDE
Common Name English
4-TOLUENESULFONYL CHLORIDE
Systematic Name English
Code System Code Type Description
HSDB
5317
Created by admin on Mon Mar 31 21:13:29 GMT 2025 , Edited by admin on Mon Mar 31 21:13:29 GMT 2025
PRIMARY
EPA CompTox
DTXSID1052660
Created by admin on Mon Mar 31 21:13:29 GMT 2025 , Edited by admin on Mon Mar 31 21:13:29 GMT 2025
PRIMARY
FDA UNII
027KYN78B4
Created by admin on Mon Mar 31 21:13:29 GMT 2025 , Edited by admin on Mon Mar 31 21:13:29 GMT 2025
PRIMARY
NSC
175822
Created by admin on Mon Mar 31 21:13:29 GMT 2025 , Edited by admin on Mon Mar 31 21:13:29 GMT 2025
PRIMARY
PUBCHEM
7397
Created by admin on Mon Mar 31 21:13:29 GMT 2025 , Edited by admin on Mon Mar 31 21:13:29 GMT 2025
PRIMARY
ECHA (EC/EINECS)
202-684-8
Created by admin on Mon Mar 31 21:13:29 GMT 2025 , Edited by admin on Mon Mar 31 21:13:29 GMT 2025
PRIMARY
MESH
C025506
Created by admin on Mon Mar 31 21:13:29 GMT 2025 , Edited by admin on Mon Mar 31 21:13:29 GMT 2025
PRIMARY
MERCK INDEX
m10963
Created by admin on Mon Mar 31 21:13:29 GMT 2025 , Edited by admin on Mon Mar 31 21:13:29 GMT 2025
PRIMARY Merck Index
WIKIPEDIA
4-TOLUENESULFONYL CHLORIDE
Created by admin on Mon Mar 31 21:13:29 GMT 2025 , Edited by admin on Mon Mar 31 21:13:29 GMT 2025
PRIMARY
CAS
98-59-9
Created by admin on Mon Mar 31 21:13:29 GMT 2025 , Edited by admin on Mon Mar 31 21:13:29 GMT 2025
PRIMARY
NIH
NCATS
PRIVACY NOTICE
ACCESSIBILITY
DISCLAIMER
HHS VULNERABILITY DISCLOSURE
For language access assistance, contact the NCATS Public Information Officer
National Center for Advancing Translational Sciences (NCATS),
6701 Democracy Boulevard, Bethesda MD 20892-4874 • 301-594-8966