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77811-09-7

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77811-09-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77811-09-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,8,1 and 1 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 77811-09:
(7*7)+(6*7)+(5*8)+(4*1)+(3*1)+(2*0)+(1*9)=147
147 % 10 = 7
So 77811-09-7 is a valid CAS Registry Number.

77811-09-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl undeca-2,4-dienoate

1.2 Other means of identification

Product number -
Other names 2E,4E-Methyl deca-2,4-dienoate

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:77811-09-7 SDS

77811-09-7Downstream Products

77811-09-7Relevant articles and documents

Palladium-catalyzed cross-coupling of aryl and alkenyl boronic acids with alkenes via oxidative addition of a carbon-boron bond to palladium(0)

Cho, Chan Sik,Uemura, Sakae

, p. 85 - 92 (2007/10/02)

Arylboronic acids react with alkenes in acetic acid at 25 deg C in the presence of a catalytic amount of palladium(II) acetate together with sodium acetate to give the corresponding aryl-substituted alkenes in high yields.Alkenylboronic acids react with alkenes under similar conditions to give the corresponding conjugated dienes stereospecifically, but the product yields are lower, compared with those from arylboronic acids.Similar treatment of sodium tetraphenylborate (NaBPh4) with alkenes also affords the corresponding phenylated alkenes in high yields together with biphenyl and benzene as side products.Oxidative addition of a carbon-boron bond to palladium(0), formed in situ, to give an organopalladium(II) species is assumed to be the key step of these cross-coupling reactions. Key words: Boronic acid; Aryl; Alkenyl; Alkene; Palladium; Oxidative addition

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