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N-ethyl-N-[(propan-2-ylsulfanyl)methyl]ethanamine is an organic compound with the molecular formula C7H17NS. It is a colorless liquid at room temperature and is soluble in organic solvents. This chemical is primarily used as a synthetic intermediate in the production of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is also known for its potential applications in the synthesis of certain dyes and pigments. Due to its reactivity, it is essential to handle N-ethyl-N-[(propan-2-ylsulfanyl)methyl]ethanamine with care, following proper safety protocols to minimize any potential hazards.

6631-70-5

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6631-70-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6631-70-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,3 and 1 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6631-70:
(6*6)+(5*6)+(4*3)+(3*1)+(2*7)+(1*0)=95
95 % 10 = 5
So 6631-70-5 is a valid CAS Registry Number.

6631-70-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-ethyl-N-(propan-2-ylsulfanylmethyl)ethanamine

1.2 Other means of identification

Product number -
Other names Diaethyl-(isopropylmercapto-methyl)-amin

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:6631-70-5 SDS

6631-70-5Downstream Products

6631-70-5Relevant academic research and scientific papers

Synthesis of amino sulfides in the presence of rare-earth and transition metal catalysts

Khairullina, R. R.,Akmanov, B. F.,Kunakova, R. V.,Ibragimov, A. G.

, p. 902 - 907,6 (2020/08/31)

Efficient procedures have been developed for the synthesis of amino sulfides by aminomethylation of thiols with higher geminal diamines, thiomethylation of secondary amines with N,N-dimethylaminomethyl sulfides, and decyclization of 1,3,6-oxadithiepane or

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