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ETHYL 6-(3-CHLOROPHENYL)-6-OXOHEXANOATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

333355-35-4

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333355-35-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 333355-35-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,3,3,5 and 5 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 333355-35:
(8*3)+(7*3)+(6*3)+(5*3)+(4*5)+(3*5)+(2*3)+(1*5)=124
124 % 10 = 4
So 333355-35-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H17ClO3/c1-2-18-14(17)9-4-3-8-13(16)11-6-5-7-12(15)10-11/h5-7,10H,2-4,8-9H2,1H3

333355-35-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 6-(3-chlorophenyl)-6-oxohexanoate

1.2 Other means of identification

Product number -
Other names 5-chlorobenzoyl valeric acid,ethyl ester

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:333355-35-4 SDS

333355-35-4Relevant academic research and scientific papers

Pd(OH)2/C (Pearlman's catalyst): A highly active catalyst for Fukuyama, Sonogashira, and Suzuki coupling reactions

Mori, Yoshikazu,Seki, Masahiko

, p. 1571 - 1574 (2007/10/03)

Treatment of thiol esters 1 with zinc reagent 2 in the presence of a small amount (2/C (Pearlman's catalyst) provided functionalized asymmetrical ketones 3 in high yields. The use of Pd(OH)2/C was

Palladium on charcoal-catalyzed Fukuyama coupling reaction

Shimizu, Toshiaki,Seki, Masahiko

, p. 429 - 432 (2007/10/03)

The Pd/C-catalyzed coupling reactions of thiol esters 1 with a zinc reagent 2 were accomplished in the presence of DMF leading to the polyfunctional ketones 3 in good yields under mild reaction conditions. The protocol was applied to the coupling reaction of a thiolactone 4c with a zinc reagent 2 to provide, after dehydration, a dehydrobiotin derivative 5c in 94% yield.

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