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1,2,5,6-Dithiadiazocine-4,7(3H,8H)-dione,dihydro-5,6-dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

131760-68-4

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131760-68-4 Usage

Chemical class

Dithiadiazocine

Structural type

Heterocyclic organic compound

Ring composition

Six-membered ring with two nitrogen atoms, two sulfur atoms, and two oxygen atoms

Form

Dihydro-5,6-dimethyl

Applications

a. Production of pharmaceuticals
b. Production of agrochemicals
c. Synthesis of other organic compounds
d. Potential use in materials science
e. Potential use in catalysis

Research interest

Unique structural and chemical properties

Check Digit Verification of cas no

The CAS Registry Mumber 131760-68-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,7,6 and 0 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 131760-68:
(8*1)+(7*3)+(6*1)+(5*7)+(4*6)+(3*0)+(2*6)+(1*8)=114
114 % 10 = 4
So 131760-68-4 is a valid CAS Registry Number.

131760-68-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-dimethyl-3,8-dioxo-1,2,5,6-diazadithiocane

1.2 Other means of identification

Product number -
Other names Hexahydro N,N'dimethyl-4,7-dioxo-1,2-dithia-5,6-diazocine

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:131760-68-4 SDS

131760-68-4Relevant academic research and scientific papers

A Reagent for Reduction of Disulfide Bonds in Proteins That Reduces Disulfide Bonds Faster Than Does Dithiothreitol

Singh, Rajeeva,Whitesides, George M.

, p. 2332 - 2337 (2007/10/02)

We have synthesized a new reagent - N,N'-dimethyl-N,N'-bis(mercaptoacetyl)hydrazine (DMH) - for the reduction of disulfide bonds in proteins.DMH reduces disulfide bonds 7 times faster than does dithiothreitol (DTT) in water at pH 7.DMH reduces mixed disulfides of cysteine proteases (papain and ficin) especially rapidly (30 times faster than DTT).DMH (ε0 = -0.300 V) reduces noncyclic disulfides completely, although it is less strongly reducing than DTT (ε0 = -0.356 V).

meso-2,5-Dimercapto-N,N,N',N'-tetramethyladipamide: A Readily Available, Kinetically Rapid Reagent for the Reduction of Disulfides in Aqueous Solution

Lees, Watson J.,Singh, Rajeeva,Whitesides, George M.

, p. 7328 - 7331 (2007/10/02)

meso-2,5-Dimercapto-N,N,N',N'-tetramethyladipamide (meso-DTA) reduces disulfide bonds up to 8 times faster (kinetic) than does dithiothreitol (DTT) in aqueous solution at pH 7.0. meso-DTA is easily synthesized in five steps (39percent overall yield) from adipic acid. meso-DTA, which forms a cyclic disulfide, is less reducing than DTT by approximately 56 mV, but is much more reducing than mercaptoethanol.

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