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129101-37-7

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129101-37-7 Usage

Uses

(2R)-6-Fluoro-3,4-dihydro-2H-1-benzopyran-2-carboxylic acid is a useful reagent for organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 129101-37-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,1,0 and 1 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 129101-37:
(8*1)+(7*2)+(6*9)+(5*1)+(4*0)+(3*1)+(2*3)+(1*7)=97
97 % 10 = 7
So 129101-37-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H9FO3/c11-7-2-4-8-6(5-7)1-3-9(14-8)10(12)13/h2,4-5,9H,1,3H2,(H,12,13)/t9-/m1/s1

129101-37-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R)-6-fluoro-3,4-dihydro-2H-chromene-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names -

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:129101-37-7 SDS

129101-37-7Relevant articles and documents

Preparation method of chromanone 2-carboxylic acid or chroman 2-carboxylic acid derivatives

-

, (2017/05/16)

The present invention relates to a chromanone-2-carboxylic acid derivative and a chroman-2-carboxylic acid derivative which can be used as an intermediate for effective medicinal components currently available in the market, and to preparation methods the

PROCESS FOR THE PREPARATION OF NEBIVOLOL

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Page/Page column 16-18, (2012/07/28)

The present invention relates to a novel process for the synthesis of the Nebivolol product depicted in Scheme 1, comprised of a reduced number of high-yield steps, and characterized by the enzymatic resolution of the chroman ester precursor.

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