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53575-08-9

53575-08-9

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53575-08-9 Usage

Chemical Properties

clear yellow liquid

Uses

Diethyl 1-Naphthylmethylphosphonate is an intermediate used to prepare dual inhibitors of leukocyte proteases cathepsin G and chymase.

Check Digit Verification of cas no

The CAS Registry Mumber 53575-08-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,5,7 and 5 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 53575-08:
(7*5)+(6*3)+(5*5)+(4*7)+(3*5)+(2*0)+(1*8)=129
129 % 10 = 9
So 53575-08-9 is a valid CAS Registry Number.
InChI:InChI=1/C15H19O3P/c1-3-17-19(16,18-4-2)12-14-10-7-9-13-8-5-6-11-15(13)14/h5-11H,3-4,12H2,1-2H3

53575-08-9 Well-known Company Product Price

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  • Alfa Aesar

  • (L05286)  Diethyl 1-naphthylmethylphosphonate, 95%   

  • 53575-08-9

  • 10g

  • 1379.0CNY

  • Detail

  • Alfa Aesar

  • (L05286)  Diethyl 1-naphthylmethylphosphonate, 95%   

  • 53575-08-9

  • 50g

  • 5756.0CNY

  • Detail

53575-08-9SDS

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 DIETHYL 1-NAPHTHYLMETHYLPHOSPHONATE

1.2 Other means of identification

Product number -
Other names Diethyl 1-naphthylmethylphosphonate

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:53575-08-9 SDS

53575-08-9Relevant articles and documents

Preparation des acides alkyl et arylalkyl-5 methyl-2 benzofurannedicarboxyliques-6,7. Application a la synthese de derives de nouveaux heterocycles

Cabares, Jacques,Mavoungou-Gomes, Louis

, p. 401 - 412 (2007/10/02)

Direct formation of 5-alkyl or arylalkyl 2-methylbenzofuran 6,7-dicarboxylic acid derivatives from Diels-Alder adducts of 5-alkyl or arylalkyl 2-acetonylfurans and dimethyl acetylenedicarboxylate is promoted by boron trifluoride etherate in methylene chloride at room temperature.The structures of these new compounds were established from their 1H and 13C nmr spectra.In 1,1,2,2-tetrachloroethane and in the presence of aluminium chloride, 5-arylalkylbenzofuran anhydrides undergo an intramolecular Friedel-Crafts acylations leading to new polycyclic benzofuran derivatives.

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