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2H-Pyran-2-one, 6-[(1S)-2-[[(1,1-dimethylethyl)diphenylsilyl]oxy]-1-methylethyl]tetrahydro- 5-methyl-, (5S,6S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

237735-80-7

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237735-80-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 237735-80-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,7,7,3 and 5 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 237735-80:
(8*2)+(7*3)+(6*7)+(5*7)+(4*3)+(3*5)+(2*8)+(1*0)=157
157 % 10 = 7
So 237735-80-7 is a valid CAS Registry Number.

237735-80-7SDS

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 (5S,6S)-6-{(1S)-2-[(tert-butyldiphenylsilyl)oxy]-1-methylethyl}-5-methyltetrahydro-2H-pyran-2-one

1.2 Other means of identification

Product number -
Other names (5S,6S)-6-[(S)-2-(tert-Butyl-diphenyl-silanyloxy)-1-methyl-ethyl]-5-methyl-tetrahydro-pyran-2-one

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:237735-80-7 SDS

237735-80-7Relevant academic research and scientific papers

Formal total synthesis of (+)-methynolide

Cossy, Janine,Bauer, David,Bellosta, Véronique

, p. 5909 - 5922 (2007/10/03)

A formal total synthesis of (+)-methynolide was achieved in 23 steps highlighted by a crotylboration, a ring-closing metathesis, a Sharpless kinetic resolution of an allylic alcohol and a Takai reaction.

A short synthesis of the C1-C7 fragment of methymycin by ring-closing olefin metathesis

Cossy,Bauer,Bellosta

, p. 4187 - 4188 (2007/10/03)

The synthesis of the C1-C7 fragment of methymycin was achieved via a ring-closing olefin metathesis employing Grubb's catalyst in the presence of Ti(OiPr)4.

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