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Benzenethiol, 4-(dimethylamino)-, sodium salt is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

25661-63-6

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25661-63-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25661-63-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,6,6 and 1 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 25661-63:
(7*2)+(6*5)+(5*6)+(4*6)+(3*1)+(2*6)+(1*3)=116
116 % 10 = 6
So 25661-63-6 is a valid CAS Registry Number.

25661-63-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name sodium 4-N,N-dimethylaminobenzenethiolate

1.2 Other means of identification

Product number -
Other names Sodium

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:25661-63-6 SDS

25661-63-6Relevant academic research and scientific papers

Controlling O2 Reactivity in Synthetic Analogues of [NiFeS]- And [NiFeSe]-Hydrogenase Active Sites

Yang, Xuemei,Elrod, Lindy C.,Le, Trung,Vega, Valeria S.,Naumann, Haley,Rezenom, Yohannes,Reibenspies, Joseph H.,Hall, Michael B.,Darensbourg, Marcetta Y.

, p. 15338 - 15347 (2019)

Strategies for limiting, or reversing, the degradation of air-sensitive, base metal catalysts for the hydrogen evolution/oxidation reaction on contact with adventitious O2 are guided by nature′s design of hydrogenase active sites. The affinity

PHOTOCHEMICAL SUBSTITUTION OF HALOGEN AND SO2X GROUPS BY THIOUREA AND THIOSEMICARBAZIDE. PHOTOSYNTHESIS OF AROMATIC DISULFIDES

Frolov, A. N.,Klokova, E. M.,El'tsov, A. V.

, p. 1926 - 1935 (2007/10/02)

During UV irradiation in the presence of thiourea (or thiosemicarbazide) the para- and ortho-halogen and sulfonyl derivatives of the benzene, naphthalene, and heterocyclic series with donating substituents in the ring are converted into arylisothiuronium salts.Thermal hydrolysis and oxidation of these salts lead to the formation of the respective diaryl disulfides in the case of the para isomers and thiazoles for the ortho isomers.

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