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4H-1-Benzopyran-4-one, 3-(cyclohexylamino)-2-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

37816-09-4

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37816-09-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 37816-09-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,8,1 and 6 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 37816-09:
(7*3)+(6*7)+(5*8)+(4*1)+(3*6)+(2*0)+(1*9)=134
134 % 10 = 4
So 37816-09-4 is a valid CAS Registry Number.

37816-09-4SDS

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 3-(cyclohexylamino)-2-phenylchromen-4-one

1.2 Other means of identification

Product number -
Other names 3-cyclohexylaminoflavone

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:37816-09-4 SDS

37816-09-4Downstream Products

37816-09-4Relevant academic research and scientific papers

Synthesis of 3-aminoflavones from 3-hydroxyflavones via 3-tosyloxy- or 3-mesyloxyflavones

Takechi, Atsushi,Takikawa, Hirosato,Miyake, Hideyoshi,Sasaki, Mitsuru

, p. 128 - 129 (2007/10/03)

Reaction of 3-tosyloxy- or 3-mesyloxyflavones with ammonia or primary amines proceeded to give the corresponding 3-aminoflavones in high yields. 3-Aminoluteorin was efficiently prepared from rutin using this method. Copyright

Amine-effected cyclization of chalcone dihalides to aurones

Donnelly, John A.,Emerson, Geraldine M.

, p. 7227 - 7236 (2007/10/02)

The possibility of employing the amine-catalysed cyclization of αβ-dibromodihydrochalcones and α-bromochalcones as a general synthesis of aurones was studied using cyclohexylamine and the most representative member of each class of these αβ-disubstituted ketones and α-halogeno chalcones. Overall yields of heterocyclic products were generally poor except from 4′6′-dimethoxy- and 3-nitro-substituted chalcone systems; aurones were obtained in fair yield from the former and in excellent yield from the latter. 22′-Diacetoxychalcone dibromide and 22′-diacetoxy-α-bromochalcone cyclised to a 2-benzoylbenzofuran to the exclusion of the corresponding aurone and flavone.

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