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38447-82-4

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38447-82-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38447-82-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,4,4 and 7 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 38447-82:
(7*3)+(6*8)+(5*4)+(4*4)+(3*7)+(2*8)+(1*2)=144
144 % 10 = 4
So 38447-82-4 is a valid CAS Registry Number.

38447-82-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methylthian-4-ol

1.2 Other means of identification

Product number -
Other names 4-Hydroxy-4-methyltetrahydro-2(H)-thiapyran

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:38447-82-4 SDS

38447-82-4Downstream Products

38447-82-4Relevant articles and documents

Scalable preparation of 4,4-disubstituted six-membered cyclic sulfones

Hugelshofer, Cedric L.,Bao, Jianming,Du, Juana,Ashley, Eric,Yu, Wensheng,Ji, Tao,Hu, Bin,Liu, Dejun,Rondla, Ramu,Karampuri, Srinivas,Sharma, Vishal,Ethiraj, Krishna,Lim, Yeon-Hee

, p. 943 - 947 (2021)

We provide an account of synthetic strategies aimed at the efficient preparation of 4-amino-4-methyltetrahydro-2H-thiopyran 1,1-dioxide (3), an important cyclic sulfone building block for medicinal chemistry. A practical and scalable protocol has been developed that readily gives access to the title compound from commercially available and inexpensive starting materials. In addition, this novel approach has enabled the synthesis of various related 4,4-disubstituted cyclic sulfone derivatives that serve as valuable structural motifs for drug discovery.

Di(2-pyridyl) carbonate promoted alkoxycarbonylation of amines: A convenient synthesis of functionalized carbamates

Ghosh, Arun K.,Duong, Tien T.,McKee, Scan P.

, p. 4251 - 4254 (2007/10/02)

The reaction of di(2-pyridyl) carbonate with a variety of alcohols including hindered secondary, tertiary and protected glycols afforded the corresponding mixed carbonate which was efficiently transformed into various carbamates in high yield under mild c

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