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49660-57-3

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49660-57-3 Usage

Chemical Properties

Pale yellow crystalline solid

Check Digit Verification of cas no

The CAS Registry Mumber 49660-57-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,6,6 and 0 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 49660-57:
(7*4)+(6*9)+(5*6)+(4*6)+(3*0)+(2*5)+(1*7)=153
153 % 10 = 3
So 49660-57-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H7BrO2/c10-6-1-2-9-7(5-6)8(11)3-4-12-9/h1-2,5H,3-4H2

49660-57-3 Well-known Company Product Price

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  • Aldrich

  • (732788)  6-Bromo-4-chromanone  

  • 49660-57-3

  • 732788-250MG

  • 1,630.98CNY

  • Detail

49660-57-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-Bromo-2,3-Dihydro-4H-Chromen-4-One

1.2 Other means of identification

Product number -
Other names 6-Bromochroman-4-one

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:49660-57-3 SDS

49660-57-3Relevant articles and documents

Acid activated montmorillonite K-10 mediated intramolecular acylation: Simple and convenient synthesis of 4-chromanones

Begum, Ayisha F.,Balasubramanian, Kalpattu K.,Shanmugasundaram, Bhagavathy

supporting information, (2021/09/13)

3-Aryloxyproionic acids undergo intramolecular cyclization in the presence of AA.Mont.K-10 in toluene under reflux for 30–45 min in good to excellent yields. Phenyl ring bearing various substituents at the ortho, meta, para positions undergo this cyclization reaction. This method involves simple work up and amenable for large scale preparations. The heterogeneous acid treated catalyst can be regenerated and used for up to three cycles with minimum loss of activity.

Chemoselective Hydrosilylation of the α,β-Site Double Bond in α,β- And α,β,γ,δ-Unsaturated Ketones Catalyzed by Macrosteric Borane Promoted by Hexafluoro-2-propanol

Zhan, Xiao-Yu,Zhang, Hua,Dong, Yu,Yang, Jian,He, Shuai,Shi, Zhi-Chuan,Tang, Lei,Wang, Ji-Yu

, p. 6578 - 6592 (2020/07/17)

The B(C6F5)3-catalyzed chemoselective hydrosilylation of α,β- and α,β,γ,δ-unsaturated ketones into the corresponding non-symmetric ketones in mild reaction conditions is developed. Nearly 55 substrates including those bearing reducible functional groups such as alkynyl, alkenyl, cyano, and aromatic heterocycles are chemoselectively hydrosilylated in good to excellent yields. Isotope-labeling studies revealed that hexafluoro-2-propanol also served as a hydrogen source in the process.

A new method for the synthesis of six bromine four hydrogen colors chromone (by machine translation)

-

Paragraph 0022; 0035, (2017/07/13)

The invention discloses a method for synthesizing six bromine four hydrogen colors recombination, is in the reaction solvent, to phenol and acrylonitrile reaction raw material, under the action of the organic drugs, six bromine four hydrogen colors recombination reaction. The invention mild reaction conditions, cheap raw material, the value of the product is very high. This invention synthetic six bromine four hydrogen colors recombination has very high medicinal value, conducive to diabetes, obesity, disorders of the nervous system in the fields of research and development of new drugs, has extensive use and application market. (by machine translation)

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