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Bis(2,2-dimethylpropyl) sulfite, also known as diisobutylsulfite, is an organic compound with the chemical formula C8H18O3S. It is a colorless liquid that is soluble in organic solvents and has a mild, sulfurous odor. bis(2,2-dimethylpropyl) sulfite is primarily used as a reducing agent in various chemical reactions, particularly in the synthesis of pharmaceuticals and agrochemicals. It is also employed as a stabilizer in the production of polymers and as an intermediate in the preparation of other sulfur-containing compounds. Due to its reactivity, bis(2,2-dimethylpropyl) sulfite is handled with care, as it can be harmful if inhaled, ingested, or absorbed through the skin.

6291-08-3

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6291-08-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6291-08-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,9 and 1 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6291-08:
(6*6)+(5*2)+(4*9)+(3*1)+(2*0)+(1*8)=93
93 % 10 = 3
So 6291-08-3 is a valid CAS Registry Number.

6291-08-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Neopentyl sulfite

1.2 Other means of identification

Product number -
Other names sulfurous acid dineopentyl ester

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:6291-08-3 SDS

6291-08-3Downstream Products

6291-08-3Relevant articles and documents

REACTIONS OF N-SULFINYL-p-TOLUENESULFONAMIDE WITH ALCOHOLS

McFarland, John W.,Schut, Dirk,Zwanenburg, Binne

, p. 389 - 393 (2007/10/02)

N-Sulfinyl-p-toluenesulfonamide (1) reacted with triaryl- and diarylmethanols to give predominantly N-substituted sulfonamides and SO2 presumably via carbonium ion intermediates.When carbonium ion forming alcohols, such as t-BuOH and Ph2C(Me)OH, were used, the predominant products were alkenes and p-toluenesulfonamide.Allylic alcohols afforded N-substituted sulfonamides, along with dienes and p-toluenesulfonamide.Alcohols wich could not predictably give relatively stable intermediate carbonium ions, gave either dialkyl sulfites or dialkyl ethers, along with p-toluenesulfonamide.In one case, namely with 9-phenylfluorenol, the 1:1 adduct with 1 (an amidosulfite) was isolated.A mechanism for the reaction is proposed.

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