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Phosphonic acid, (2-chlorobenzoyl)-, dimethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

76387-49-0

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76387-49-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76387-49-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,3,8 and 7 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 76387-49:
(7*7)+(6*6)+(5*3)+(4*8)+(3*7)+(2*4)+(1*9)=170
170 % 10 = 0
So 76387-49-0 is a valid CAS Registry Number.

76387-49-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-chlorophenyl)-dimethoxyphosphorylmethanone

1.2 Other means of identification

Product number -
Other names Dimethyl 2-chlorobenzoylphosphonate

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:76387-49-0 SDS

76387-49-0Relevant academic research and scientific papers

Hetero Diels-Alder reactions of acyl phosphonates: Synthesis of glycosyl type phosphonates

Polat-Cakir, Sidika,Demir, Ayhan S.

body text, p. 2396 - 2401 (2011/04/26)

We have prepared glycosyl type phosphonates via hetero Diels-Alder (HDA) reactions of acyl phosphonates with electron rich dienes. HDA reactions of acyl phosphonates with Danishefsky's diene required thermal activation to yield the desired dihydropyranone

Reactions of acyl phosphonates with organoaluminum reagents: A new method for the synthesis of secondary and tertiary α-hydroxy phosphonates

Seven, Ozlem,Polat-Cakir, Sidika,Hossain, Md. Shakhawoat,Emrullahoglu, Mustafa,Demir, Ayhan S.

body text, p. 3464 - 3469 (2011/06/19)

The reactions of organoaluminum reagents (trimethylaluminum, triethylaluminum, etc.) with aryl and alkyl acyl phosphonates, which lead to the formation of α-hydroxy phosphonates in moderate to good yields, are reported. This method provides easy access to

Dialkyl phosphonates and tetraalkyl bis(phosphonate)s from the decomposition of quasi-phosphonium ylidic phosphonates in aqueous conditions

Griffiths, D. Vaughan,Karim, Khalku,Harris, Jayne E.

, p. 2539 - 2544 (2007/10/03)

The reaction of dimethyl benzoylphosphonates 1 (X = 2-halogen or 2-CF3O) with trialkyl phosphite leads to the formation of carbene intermediates 3 which are trapped by trialkyl phosphite to give the corresponding ylidic phosphonates 4. In acidi

Asymmetric Synthesis of Chiral, Nonracemic Dialkyl α-Hydroxyarylmethyl- and α-, β- and γ-Hydroxyalkylphosphonates from Keto Phosphonates

Meier, Chris,Laux, Wolfgang H. G.,Bats, Jan W.

, p. 1963 - 1980 (2007/10/03)

The enantioselective synthesis of α-hydroxyarylmethylphosphonates 2a-p by the oxazaborolidine-catalyzed reduction of α-keto phosphonates 1a-p using different boranes 4a-c was studied in detail.Moderate to good enantioselectivities are found (up to 80perce

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