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Octanamide, 8-bromo- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88785-06-2

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88785-06-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88785-06-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,7,8 and 5 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 88785-06:
(7*8)+(6*8)+(5*7)+(4*8)+(3*5)+(2*0)+(1*6)=192
192 % 10 = 2
So 88785-06-2 is a valid CAS Registry Number.

88785-06-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-bromooctanamide

1.2 Other means of identification

Product number -
Other names Octanamide,8-bromo

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:88785-06-2 SDS

88785-06-2Relevant academic research and scientific papers

Palladium-catalyzed regiodivergent hydroaminocarbonylation of alkenes to primary amides with ammonium chloride

Gao, Bao,Zhang, Guoying,Zhou, Xibing,Huang, Hanmin

, p. 380 - 386 (2018)

Palladium-catalyzed hydroaminocarbonylation of alkenes for the synthesis of primary amides has long been an elusive aim. Here, we report an efficient catalytic system which enables inexpensive NH4Cl to be utilized as a practical alternative to gaseous ammonia for the palladium-catalyzed alkene-hydroaminocarbonylation reaction. Through appropriate choice of the palladium precursors and ligands, either branched or linear primary amides can be obtained in good yields with good to excellent regioselectivities. Primary mechanistic studies were conducted and disclosed that electrophilic acylpalladium species were capable of capturing the NH2-moiety from ammonium salts to form amides in the presence of CO with NMP as a base.

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