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61639-74-5

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61639-74-5 Usage

Chemical structure

A complex structure consisting of an isoindoline-1,3-dione ring and a 2-nitrophenylthio group.

Usage

Primarily used as a reagent in organic synthesis and pharmaceutical research.

Potential

Serves as a building block for the creation of various biologically active compounds and materials.

Reactivity

The 2-nitrophenylthio group is known for its ability to undergo various chemical reactions.

Stability

The isoindoline-1,3-dione ring provides a stable and versatile structural framework.

Versatility

The structural framework allows for the formation of diverse chemical structures.

Importance

2-(2-nitrophenylthio)isoindoline-1,3-dione is considered an important chemical compound in the field of organic chemistry and drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 61639-74-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,6,3 and 9 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 61639-74:
(7*6)+(6*1)+(5*6)+(4*3)+(3*9)+(2*7)+(1*4)=135
135 % 10 = 5
So 61639-74-5 is a valid CAS Registry Number.

61639-74-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-nitrophenyl)sulfanylisoindole-1,3-dione

1.2 Other means of identification

Product number -
Other names N-2-nitrophenylsulfenylphthalimide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:61639-74-5 SDS

61639-74-5Relevant articles and documents

OXIDATIVE IMIDATION OF N-ARYLSULFONYLARENESULFENAMIDES. N-IMIDES

Koval', I. V.,Oleinik, T. G.,Timoshin, M. Yu.

, p. 418 - 421 (2007/10/02)

The reaction of the sodium salts of N-arylsulfonylarenesulfenamides with N-halogenoimides and also with chlorine in the presence of the imides gave N-imides. Their spectral characteristics and biological activity were studied.

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