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935534-38-6

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935534-38-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 935534-38-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,5,5,3 and 4 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 935534-38:
(8*9)+(7*3)+(6*5)+(5*5)+(4*3)+(3*4)+(2*3)+(1*8)=186
186 % 10 = 6
So 935534-38-6 is a valid CAS Registry Number.

935534-38-6SDS

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 2-[tert-butyl(dimethyl)silyl]oxy-1-(4-fluorophenyl)ethanone

1.2 Other means of identification

Product number -
Other names -

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:935534-38-6 SDS

935534-38-6Relevant articles and documents

Green organocatalytic α-hydroxylation of ketones

Voutyritsa, Errika,Theodorou, Alexis,Kokotos, Christoforos G.

, p. 5708 - 5713 (2016/07/06)

An efficient and green method for the α-hydroxylation of substituted ketones has been developed. This method includes the in situ conversion of various ketones into the corresponding silyl enol ethers and their oxidation to the corresponding α-hydroxy ketones. Two protocols have been established leading either to protected α-hydroxy carbonyls or free α-hydroxy ketones. Both procedures are easy to follow and lead to good to high yields for a variety of ketones.

AZETIDINONE COMPOUNDS AND MEDICAL USE THEREOF

-

, (2012/06/30)

Preparation of azetidinone compounds and medical use thereof are provided by the present invention. More particularly, azetidionne compounds, shown as formula (I), wherein R1, R2, R3, R4, R5and R

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