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102616-13-7

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102616-13-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102616-13-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,6,1 and 6 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 102616-13:
(8*1)+(7*0)+(6*2)+(5*6)+(4*1)+(3*6)+(2*1)+(1*3)=77
77 % 10 = 7
So 102616-13-7 is a valid CAS Registry Number.

102616-13-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name (2E,4R,5R,6R,7E)-6,10-dimethyl-5-phenylmethoxyundeca-2,7-dien-4-ol

1.2 Other means of identification

Product number -
Other names (2E,7E)-(4R*,5R*,6R*)-6,10-dimethyl-5-(phenylmethoxy)undeca-2,7-dien-4-ol

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:102616-13-7 SDS

102616-13-7Relevant articles and documents

Stereocontrolled Synthesis of Highly Oxygenated Acyclic Systems via the Enolate Claisen Rearrangement of O-Protected Allylic Glycolates

Gould, Thomas J.,Balestra, Michael,Wittman, Mark D.,Gary, Jill A.,Rossano, Lucius T.,Kallmerten, James

, p. 3889 - 3901 (2007/10/02)

Enolate Claisen rearrangement of E- and Z-allylic glycolates yields the syn- and anti-2-alkoxy-3-alkyl 4-enoates, respectively, in good yields (60-90percent) and with high internal diastereoselectivity.Incorporation of the glycolate Claisen procedure into an iterative sequence consisting of Claisen rearrangement and homologation by addition of vinyl nucleophiles results in the efficient, stereocontrolled generation of remotely functionalized, highly oxygenated acyclic systems.This strategy is demonstrated in stereoselective syntheses of pine sawfly pheromone 42 and tocopherol side-chain intermediate 30.

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