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2,4-Pentadienal, 3-[[[(1,1-dimethylethyl)diphenylsilyl]oxy]methyl]-5-[(2S,3S,8S)-8-hydroxy- 2,3,7,9,9-pentamethyl-1,4-dioxaspiro[4.5]dec-6-en-8-yl]-, (2E,4E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

917752-76-2

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917752-76-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 917752-76-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,7,7,5 and 2 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 917752-76:
(8*9)+(7*1)+(6*7)+(5*7)+(4*5)+(3*2)+(2*7)+(1*6)=202
202 % 10 = 2
So 917752-76-2 is a valid CAS Registry Number.

917752-76-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S,3S,8S)-8-(3-[tert-butyldiphenylsiloxymethyl]penta-2,4-dienal)-2,3,7,9,9-pentamethyl-1,4-dioxaspiro[4.5]dec-6-en-8-ol

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:917752-76-2 SDS

917752-76-2Downstream Products

917752-76-2Relevant academic research and scientific papers

Concise enantioselective synthesis of abscisic acid and a new analogue

Smith, Timothy R.,Clark, Andrew J.,Clarkson, Guy J.,Taylor, Paul C.,Marsh, Andrew

, p. 4186 - 4192 (2008/09/19)

Short and high-yielding syntheses of enantiomerically pure (S)-(+) and (R)-(-)-abscisic acid are described. The syntheses proceed through key intermediates that preferentially recrystallise as single diastereoisomers for each enantiomer. This route allows the preparation of either enantiomer of abscisic acid in ca. 30% overall yield, and as demonstrated, gives access to an enantiomerically pure abscisic acid analogue. The Royal Society of Chemistry 2006.

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