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ETHYL (2S,3R)-3-(3'-DODECYLPHENYL)-2,3-DIHYDROXYPROPIONATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

309919-11-7

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309919-11-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 309919-11-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,9,9,1 and 9 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 309919-11:
(8*3)+(7*0)+(6*9)+(5*9)+(4*1)+(3*9)+(2*1)+(1*1)=157
157 % 10 = 7
So 309919-11-7 is a valid CAS Registry Number.

309919-11-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name ETHYL (2S,3R)-3-(3'-DODECYLPHENYL)-2,3-DIHYDROXYPROPIONATE

1.2 Other means of identification

Product number -
Other names 7aS) 2-carbethoxy perhydroindole hydrochloride

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:309919-11-7 SDS

309919-11-7Relevant academic research and scientific papers

Synthesis of Ceramide Analogues Having the C(4)-C(5) Bond of the Long-Chain Base as Part of an Aromatic or Heteroaromatic System

Chun, Jiong,He, Linli,Byun, Hoe-Sup,Bittman, Robert

, p. 7634 - 7640 (2007/10/03)

Two efficient and stereoselective methods are described for the preparation of aryl and heteroaryl ceramide analogues 2 and 3. The first route involves the addition of an aryllithium or a heteroaryllithium reagent (7a or 25a, respectively) to the L-serine-derived aldehyde 4, followed by hydrolysis of the oxazolidine, liberation of the amino group, and N-acylation. The second route, which was used to prepare arylceramide analogue 2 in eight steps and 28% overall yield starting with 3-bromobenzaldehyde, utilizes a Heck reaction to afford (E)-α,β-unsaturated ester 16, then osmium-catalyzed asymmetric dihydroxylation for the introduction of the desired chirality at C-2 and C-3. Regioselective α-azidation of α-O-nosyl-β-hydroxyester 18 with sodium azide, followed by LiAlH4 reduction of the azido and ester groups and N-acylation, complete the synthesis of arylceramide analogue 2.

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