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Details

Stereochemistry ACHIRAL
Molecular Formula C7H10N2O2S
Molecular Weight 186.231
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of P-TOLUENESULFONYLHYDRAZIDE

SMILES

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

InChI

InChIKey=ICGLPKIVTVWCFT-UHFFFAOYSA-N
InChI=1S/C7H10N2O2S/c1-6-2-4-7(5-3-6)12(10,11)9-8/h2-5,9H,8H2,1H3

HIDE SMILES / InChI
Molecular Formula C7H10N2O2S
Molecular Weight 186.231
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
1,3-Dipolar cycloaddition reactions of vinylidenecyclopropane-diesters with aromatic diazomethanes generated in situ.
2010-04-02
Deacetyl tenuazonic acid p-toluene-sulfonyl-hydrazone.
2009-11-21
4-Methyl-N-(3-oxo-2,3-dihydro-1,2-benzisothia-zol-2-yl)benzene-sulfonamide.
2009-01-31
Expansion by contraction: diversifying the photochemical reactivity scope of diazo-oxochlorins toward development of in situ alkylating agents.
2008-11-26
Intermolecular reactions of foiled carbenes with N-H bonds: evidence for an ylidic pathway.
2008-09-05
Protecting group free glycosidations using p-toluenesulfonohydrazide donors.
2008-08-21
Solvent free microwave synthesis and evaluation of antimicrobial activity of pyrimido[4,5-b]- and pyrazolo[3,4-b]quinolines.
2006-06-01
Preparation of alpha-diazocarbonyl compounds from beta-lapachone derivatives and other 1,2-naphthoquinones: use of the 2D NMR 1H,15N and 1H,13C HMBC techniques in assigning regiochemistry.
2006-04
C-glycosylmethylene carbenes: synthesis of anhydro-aldose tosylhydrazones as precursors; generation and a new synthetic route to exo-glycals.
2003-11-21
A mild and convenient procedure for the conversion of toxic beta-asarone into rare phenylpropanoids: 2,4,5-trimethoxycinnamaldehyde and gamma-asarone.
2002-05
Effective and highly stereoselective coupling with vinyldiazomethanes to form symmetrical trienes.
2002-01-25
Patents

Patents

04128644
7
04904764
1
04975461
1
06689884
1
07056918
1
07268232
3
07456177
4
07723330
34
07842685
4
07943776
4
08609708
3
JPH02172963A
3
JPH0481435A
2
JPH07196833A
1
JPS56161435A
1
JPS6251640A
1
JPS63125514A
1
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:06:26 GMT 2025
Edited
by admin
on Mon Mar 31 19:06:26 GMT 2025
Record UNII
LR93R5002M
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CELLMIC H
Preferred Name English
P-TOLUENESULFONYLHYDRAZIDE
MI  
Common Name English
4-METHYLBENZENESULFONOHYDRAZIDE
Systematic Name English
P-METHYLPHENYLSULFONYLHYDRAZINE
Common Name English
NSC-18715
Code English
4-TOLUENESULFONOHYDRAZINE
Common Name English
(P-TOLYLSULFONYL)HYDRAZINE
Common Name English
TOLUENE-4-SULPHONYL HYDRAZIDE
Common Name English
P-TOLUENESULFONIC HYDRAZIDE
Common Name English
P-TOSYLHYDRAZINE
Common Name English
POROFOR TSH 75
Brand Name English
TOLUENESULFONYL HYDRAZIDE, P-
Common Name English
4-METHYLPHENYLSULFONYL HYDRAZIDE
Common Name English
P-TOLYLSULFONYL HYDRAZIDE
Common Name English
(4-METHYLPHENYLSULFONYL)HYDRAZINE
Systematic Name English
N-TOSYLHYDRAZINE
Systematic Name English
P-TOLUENESULFONYLHYDRAZIDE [MI]
Common Name English
P-METHYLBENZENESULFONIC ACID HYDRAZIDE
Common Name English
4-METHYLBENZENESULFONYL HYDRAZIDE
Common Name English
TOLUENE-4-SULFONOHYDRAZIDE
Systematic Name English
TOLUENE-4-SULFONYL HYDRAZIDE
Common Name English
P-TOLUENESULFONHYDRAZIDE
Common Name English
4-TOLUENESULFONIC ACID HYDRAZIDE
Systematic Name English
4-METHYLBENZENESULFONIC ACID HYDRAZIDE
Systematic Name English
P-TOSYL HYDRAZIDE
Common Name English
P-METHYLBENZENESULFONYLHYDRAZINE
Common Name English
P-TOLUENESULFONYLHYDRAZINE
Common Name English
BENZENESULFONIC ACID, 4-METHYL-, HYDRAZIDE
Systematic Name English
TOSYLHYDRAZINE
Systematic Name English
P-TOLUENESULFONYL HYDRAZIDE
Common Name English
(4-TOLYLSULFONYL)HYDRAZIDE
Common Name English
P-TOLUENESULFONOHYDRAZIDE
Common Name English
TOSYLHYDRAZIDE
Common Name English
P-TOLUENESULFONIC ACID, HYDRAZIDE
Systematic Name English
Code System Code Type Description
NSC
18715
Created by admin on Mon Mar 31 19:06:26 GMT 2025 , Edited by admin on Mon Mar 31 19:06:26 GMT 2025
PRIMARY
ECHA (EC/EINECS)
216-407-3
Created by admin on Mon Mar 31 19:06:26 GMT 2025 , Edited by admin on Mon Mar 31 19:06:26 GMT 2025
PRIMARY
MERCK INDEX
m10964
Created by admin on Mon Mar 31 19:06:26 GMT 2025 , Edited by admin on Mon Mar 31 19:06:26 GMT 2025
PRIMARY Merck Index
FDA UNII
LR93R5002M
Created by admin on Mon Mar 31 19:06:26 GMT 2025 , Edited by admin on Mon Mar 31 19:06:26 GMT 2025
PRIMARY
CAS
1576-35-8
Created by admin on Mon Mar 31 19:06:26 GMT 2025 , Edited by admin on Mon Mar 31 19:06:26 GMT 2025
PRIMARY
PUBCHEM
15303
Created by admin on Mon Mar 31 19:06:26 GMT 2025 , Edited by admin on Mon Mar 31 19:06:26 GMT 2025
PRIMARY
EPA CompTox
DTXSID8051756
Created by admin on Mon Mar 31 19:06:26 GMT 2025 , Edited by admin on Mon Mar 31 19:06:26 GMT 2025
PRIMARY
NIH
NCATS
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