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2H-1-Benzopyran-6-ol, 3-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88039-99-0

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88039-99-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88039-99-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,0,3 and 9 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 88039-99:
(7*8)+(6*8)+(5*0)+(4*3)+(3*9)+(2*9)+(1*9)=170
170 % 10 = 0
So 88039-99-0 is a valid CAS Registry Number.

88039-99-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-phenyl-2H-chromen-6-ol

1.2 Other means of identification

Product number -
Other names 2H-1-Benzopyran-6-ol,3-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:88039-99-0 SDS

88039-99-0Downstream Products

88039-99-0Relevant academic research and scientific papers

Synthesis of coumaran-5-OLS - New model compounds for bioantioxidants

Sch?del, Uta,Habicher, Wolf D.

, p. 1049 - 1055 (2007/10/03)

Based on a Heck type reaction a new access to coumaran-5-ols has been developed. The reaction, its analytical and synthetical features as well as the nature of some by-products are discussed.

TRANSFORMATION DU CATION ISOFLAVYLIUM EN PHENYL-3 COUMARINES, ISOFLAVENES-3 ET ISOFLAVANNES

Deschamps-Vallet, Colette,Ilotse, Jean-Baptiste,Meyer-Dayan, Michele

, p. 3993 - 3996 (2007/10/02)

Isoflavylium salts 1 are key starting materials for synthesis of 3-phenyl coumarins 2,isoflav-3-enes 4 and isoflavans 5, by chemical conversions narrowsly apparented to biogenetic pathways actually recognized for natural compounds of these series.

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