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Details

Stereochemistry ACHIRAL
Molecular Formula C3H5I
Molecular Weight 167.9763
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ALLYL IODIDE

SMILES

ICC=C

InChI

InChIKey=HFEHLDPGIKPNKL-UHFFFAOYSA-N
InChI=1S/C3H5I/c1-2-3-4/h2H,1,3H2

HIDE SMILES / InChI

Molecular Formula C3H5I
Molecular Weight 167.9763
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Polarity of the transition state controls the reactivity of related charged phenyl radicals toward atom and group donors.
2001 Apr 20
6-Bromomethyl-4H-1,3-dioxin: a versatile bromomethyl vinyl ketone equivalent for heterocycle and carbocycle construction.
2002 Feb 6
Asymmetric synthesis of trans-2,3-piperidinedicarboxylic acid and trans-3,4-piperidinedicarboxylic acid derivatives.
2002 Feb 8
The stability of allyl radicals following the photodissociation of allyl iodide at 193 nm.
2006 Oct 14
Letter: Silver mediated ester bond formation in the gas phase: substrate structure is important.
2007
Cis double allylation of cyclopropenes using cyclopropylindium reagents.
2007 Jul 7
Determination of spin-orbit branching fractions in the photodissociation of halogenated hydrocarbons.
2007 May 17
The use of chiral lithium amides in the desymmetrisation of N-trialkylsilyl dimethyl sulfoximines.
2007 Oct 16
Gas-phase synthesis of the homo and hetero organocuprate anions [MeCuMe]-, [EtCuEt]-, and [MeCuR]-.
2008 Jan 23
Gas phase synthesis, structure and unimolecular reactivity of silver iodide cluster cations, Ag(n)I(m)(+) (n = 2-5, 0 < m < n).
2008 Jun 14
C-C bond coupling between the organometallic cations CH3Ag2+, CH3Cu2+ and CH3AgCu+ and allyliodide.
2009 Apr 21
Gas-phase reactivity of protonated 2-, 3-, and 4-dehydropyridine radicals toward organic reagents.
2009 Dec 10
Theoretical study on the halogen-zinc exchange reaction by using organozincate compounds.
2009 Jun 2
N-Cyclo-hexyl-N-(prop-2-en-1-yl)benzene-sulfonamide.
2009 Nov 18
Oxidation state, aggregation, and heterolytic dissociation of allyl indium reagents.
2010 May 5
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 02:08:40 GMT 2023
Edited
by admin
on Sat Dec 16 02:08:40 GMT 2023
Record UNII
46830QOA4D
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ALLYL IODIDE
MI  
Systematic Name English
3-IODOPROPYLENE
Systematic Name English
PROPENE, 3-IODO-
Systematic Name English
3-IODOPROPENE
Systematic Name English
UN1723
Code English
ALLYL IODIDE [MI]
Common Name English
3-IODO-1-PROPENE
Systematic Name English
NSC-18588
Code English
UN-1723
Code English
Code System Code Type Description
ECHA (EC/EINECS)
209-130-4
Created by admin on Sat Dec 16 02:08:40 GMT 2023 , Edited by admin on Sat Dec 16 02:08:40 GMT 2023
PRIMARY
EPA CompTox
DTXSID5060302
Created by admin on Sat Dec 16 02:08:40 GMT 2023 , Edited by admin on Sat Dec 16 02:08:40 GMT 2023
PRIMARY
NSC
18588
Created by admin on Sat Dec 16 02:08:40 GMT 2023 , Edited by admin on Sat Dec 16 02:08:40 GMT 2023
PRIMARY
FDA UNII
46830QOA4D
Created by admin on Sat Dec 16 02:08:40 GMT 2023 , Edited by admin on Sat Dec 16 02:08:40 GMT 2023
PRIMARY
CAS
556-56-9
Created by admin on Sat Dec 16 02:08:40 GMT 2023 , Edited by admin on Sat Dec 16 02:08:40 GMT 2023
PRIMARY
WIKIPEDIA
Allyl iodide
Created by admin on Sat Dec 16 02:08:40 GMT 2023 , Edited by admin on Sat Dec 16 02:08:40 GMT 2023
PRIMARY
PUBCHEM
11166
Created by admin on Sat Dec 16 02:08:40 GMT 2023 , Edited by admin on Sat Dec 16 02:08:40 GMT 2023
PRIMARY
MERCK INDEX
m1555
Created by admin on Sat Dec 16 02:08:40 GMT 2023 , Edited by admin on Sat Dec 16 02:08:40 GMT 2023
PRIMARY Merck Index