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51939-71-0

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51939-71-0 Usage

Uses

Different sources of media describe the Uses of 51939-71-0 differently. You can refer to the following data:
1. Chromane-2-carboxylic Acid is used in the synthesis of 4-quinazolinones as Rho kinase inhibitors for application towards glaucoma, hypertension and spinal cord injuries. It is also used in the prepara tion of chromanyl-benzamidazoles as anti-bacterial compounds.
2. Chromane-2-carboxylic Acid is used in the synthesis of 4-quinazolinones as Rho kinase inhibitors for application towards glaucoma, hypertension and spinal cord injuries. It is also used in the preparation of chromanyl-benzamidazoles as anti-bacterial compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 51939-71-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,9,3 and 9 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 51939-71:
(7*5)+(6*1)+(5*9)+(4*3)+(3*9)+(2*7)+(1*1)=140
140 % 10 = 0
So 51939-71-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H10O3/c11-10(12)9-6-5-7-3-1-2-4-8(7)13-9/h1-4,9H,5-6H2,(H,11,12)

51939-71-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4-dihydro-2H-chromene-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2,3-dihydrobenzopyran 2-carboxylic acid

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:51939-71-0 SDS

51939-71-0Relevant articles and documents

Model Reactions for the Enantioselective Synthesis of γ-Rubromycin: Stereospecific Intramolecular Photoredox Cyclization of an ortho-Quinone Ether to a Spiroacetal

Wakita, Fumihiro,Ando, Yoshio,Ohmori, Ken,Suzuki, Keisuke

supporting information, p. 3928 - 3932 (2018/07/25)

A model study for the enantioselective total synthesis of γ-rubromycin has revealed a promising approach for constructing the chiral, nonracemic bicyclic spiroacetal via the stereospecific photoredox reaction of 1,2-naphthoquinone ether.

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