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4H-1-Benzopyran-4-one,3-(4-morpholinyl)-2-phenyl-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81281-86-9

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81281-86-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81281-86-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,2,8 and 1 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 81281-86:
(7*8)+(6*1)+(5*2)+(4*8)+(3*1)+(2*8)+(1*6)=129
129 % 10 = 9
So 81281-86-9 is a valid CAS Registry Number.

81281-86-9SDS

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-morpholin-4-yl-2-phenylchromen-4-one

1.2 Other means of identification

Product number -
Other names 4H-1-Benzopyran-4-one,3-(4-morpholinyl)-2-phenyl

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:81281-86-9 SDS

81281-86-9Downstream Products

81281-86-9Relevant academic research and scientific papers

Synthesis of 3-N-Substituted Aminoflavones as Potential CNS Agents

Kapoor, R. P.,Rastogi, M. K.,Garg, C. P.

, p. 285 - 286 (2007/10/02)

3-N-Substituted aminoflavones (VI) have been synthesized by the action of appropriate secondary amines on 3-bromoflavone (III).In the preparation of III by a known procedure involving the bromination of flavone (II), a mixture of three products has been obtained rather than one product as reported by Pendse .The structures of VI and two of the bromination products have been established on the basis of their elemental analyses and spectral data.Compounds VI exhibit weak CNS depressant, hypotensive and hyperthermic activities.

FLAVONOIDS, XXXVI REACTION OF 3-ALKYL- OR -ARYLSULFONYLOXYFLAVANONES WITH AMINES. SYNTHESIS OF 3-DIALKYLAMINOFLAVANONES

Patonay, T.,Litkei, Gy.,Bognar, R.

, p. 135 - 146 (2007/10/02)

Reactions of 3-alkyl- or -arylsulfonyloxyflavanones (1a-h) with primary and tertiary amines gave mixtures of the corresponding flavones (2a-d) and aurones (3a-d), while with secondary amines, in addition to 2 and 3, 3-dialkylaminoflavanones (6-9) were also obtained.The factors which determine the ratio of products are discussed.Treatment of the 3-dialkylaminoflavones 6a and 7 with DDQ gave 3-dialkylaminoflavanones (10, 11); treatment with alkali in methanol afforded 2-dialkylamino-2-benzylcoumaran-3-ones (12, 13).

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