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208932-51-8

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208932-51-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 208932-51-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,8,9,3 and 2 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 208932-51:
(8*2)+(7*0)+(6*8)+(5*9)+(4*3)+(3*2)+(2*5)+(1*1)=138
138 % 10 = 8
So 208932-51-8 is a valid CAS Registry Number.

208932-51-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-hydroxyphenyl)propionic acid allyl ester

1.2 Other means of identification

Product number -
Other names allyl 3-(4-hydroxyphenyl)propanoate

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:208932-51-8 SDS

208932-51-8Relevant articles and documents

POLYMER PARTICLES

-

Paragraph 0157; 0161, (2018/04/20)

Described are polymers and methods of forming and using same.

Efficient synthesis of resin-bound α-TMSdiazoketones and their use in solid-phase organic synthesis

Iso, Yasuyoshi,Shindo, Hirohisa,Hamana, Hiroshi

, p. 5353 - 5361 (2007/10/03)

α-TMSdiazoketones on a solid support could be simply and efficiently prepared by reaction of the corresponding resin-bound acid chlorides with excess TMSdiazomethane, without any bases. These α-TMSdiazoketones were used via carbenes or carbenoids for a variety of solid-phase reactions. These useful solid-phase reactions allow efficient construction of diverse compound libraries by use of combinatorial chemistry, due to the high reactivity and wide applications of the carbenes or carbenoids. (C) 2000 Elsevier Science Ltd.

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