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6-FLUORO-2-METHYLCHROMONE 97 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75487-84-2

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75487-84-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75487-84-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,4,8 and 7 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 75487-84:
(7*7)+(6*5)+(5*4)+(4*8)+(3*7)+(2*8)+(1*4)=172
172 % 10 = 2
So 75487-84-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H7FO2/c1-6-4-9(12)8-5-7(11)2-3-10(8)13-6/h2-5H,1H3

75487-84-2 Well-known Company Product Price

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  • Aldrich

  • (543772)  6-Fluoro-2-methylchromone  97%

  • 75487-84-2

  • 543772-1G

  • 751.14CNY

  • Detail

75487-84-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-fluoro-2-methylchromen-4-one

1.2 Other means of identification

Product number -
Other names 6-Fluoro-2-methylchromone

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:75487-84-2 SDS

75487-84-2Downstream Products

75487-84-2Relevant academic research and scientific papers

Synthesis of chiral chromanols: Via a RuPHOX-Ru catalyzed asymmetric hydrogenation of chromones

Ma, Yujie,Li, Jing,Ye, Jianxun,Liu, Delong,Zhang, Wanbin

supporting information, p. 13571 - 13574 (2019/01/05)

Chiral chromanols and their derivatives have been synthesized via a RuPHOX-Ru catalyzed asymmetric hydrogenation of chromones in high yields, >20:1 drs and with up to 99.9% ee. Control experiments show that the reaction undergoes two sequential asymmetric hydrogenation steps of the CC and CO double bonds. The reaction could be performed on a gram-scale with a relatively low catalyst loading (up to 1000 S/C), and the resulting products can be transformed to several biologically active compounds.

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