DICHLORAMINE T

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

InChIKey=ARGDYOIRHYLIMT-UHFFFAOYSA-N

InChI=1S/C7H7Cl2NO2S/c1-6-2-4-7(5-3-6)13(11,12)10(8)9/h2-5H,1H3

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

PubMed

Title	Date	PubMed
One-pot highly stereoselective synthesis of cyano aziridines via the CuCl-catalyzed aminochlorination of α,β-unsaturated nitriles and intramolecular S(N) 2 substitution.	2010-11	20880018
Manganese (IV) oxide-catalyzed electrophilic diamination of electron-deficient alkenes provides an easy synthesis of alpha,beta-diamino acid and ketone derivatives for peptidomimetic studies.	2005-11	16218992
Ionic liquid media resulted in the first asymmetric aminohalogenation reaction of alkenes.	2004-12-23	15606090
Electrophilic diamination of alkenes by using FeCl(3)-PPh(3) complex as the catalyst.	2002-07-12	12098288

Substance Class	Chemical Created by `admin` on `Mon Mar 31 19:14:12 GMT 2025` Edited by `admin` on `Mon Mar 31 19:14:12 GMT 2025`
Record UNII	36XJA7756O
Record Status	`Validated (UNII)`
Record Version

Name

Type

Language

NSC-1130

Preferred Name

English

DICHLORAMINE T

Common Name

English

DICHLORAMINE T [MI]

Common Name

English

N,N-DICHLORO-4-METHYLBENZENESULFONAMIDE

Systematic Name

English

N,N-DICHLORO-P-TOLUENESULFONAMIDE

Common Name

English

P-TOLUENESULFONIC ACID DICHLORAMIDE

Common Name

English

DICHLORAMINE-T

Common Name

English

Code System Code Type Description

EPA CompTox

DTXSID6060054