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142753-40-0

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142753-40-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 142753-40-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,7,5 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 142753-40:
(8*1)+(7*4)+(6*2)+(5*7)+(4*5)+(3*3)+(2*4)+(1*0)=120
120 % 10 = 0
So 142753-40-0 is a valid CAS Registry Number.

142753-40-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl α-chloro-α-phenylseleno acetate

1.2 Other means of identification

Product number -
Other names ethyl-α-chloro-α-phenylseleno acetate

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:142753-40-0 SDS

142753-40-0Relevant articles and documents

Scandium-catalyzed carbon-carbon bond formations using α- organosulfanyl and organoselanyl-α-fluoroacetic acid derivatives

Gotoh, Kohei,Yamamoto, Teruhisa,Yoshimatsu, Mitsuhiro

, p. 1611 - 1615 (2007/10/03)

The scandium-catalyzed reactions of α-organosulfanyl and organoselanyl-α-fluoroacetates 1-2, acetamides 3-4 and acetonitrile 5 with soft nucleophiles proceeded to give the products 6a-b, 7a-c, 8a-c, 9a-e in good to high yields. We also successfully perfor

Synthesis of α-phenylchalcogeno acetic acids, ethyl-α-phenylchalcogeno acetates and ethyl-α-halo-α-phenylchalcogeno acetates

Dabdoub, Miguel J.,Guerrero, Palimecio G.,Silveira, Claudio C.

, p. 31 - 38 (2007/10/02)

Reaction of phenyltellurolate or phenylselenolate anion with α-bromoacetic acid under phase transfer conditions using a liquid-solid system affords the α-phenyltelluro acetic acid and the α-phenylseleno acetic acid in 44 and 50percent yields respectively.

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