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2555-31-9

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2555-31-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2555-31-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,5 and 5 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2555-31:
(6*2)+(5*5)+(4*5)+(3*5)+(2*3)+(1*1)=79
79 % 10 = 9
So 2555-31-9 is a valid CAS Registry Number.

2555-31-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-methoxy-4-phenylchromen-2-one

1.2 Other means of identification

Product number -
Other names 7-Methoxy-4-phenyl-cumarin

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:2555-31-9 SDS

2555-31-9Relevant articles and documents

A Facile Synthesis of 4-Aryl-2H-1-benzopyran-2-ones

Ahluwalia, Vinod K.,Singh, Daljeet,Singh, Rishi P.

, p. 869 - 872 (1985)

Reaction of 2-hydroxybenzophenones (1, 3, 7, 8) with ethoxycarbonylmethylenetriphenylphosphorane affords 4-aryl-2H-1-benzopyran-2-ones (2, 4-6) in excellent yields. - Keywords: 4-Aryl-2H-1-benzopyran-2-ones; Ethoxycarbonylmethylenetriphenylphosphorane; Friedel-Crafts reaction; 2-Hydroxybenzophenones; Wittig reaction

Photoinduced cyclization of alkynoates to coumarins with N-Iodosuccinimide as a free-radical initiator under ambient and metal-free conditions

Wang, Zhihui,Li, Xuezhi,Wang, Lei,Li, Pinhua

, p. 1044 - 1051 (2019/01/25)

An efficient photoinduced strategy for the preparation of coumarins was developed. In the presence of N-iodosuccinimide (NIS) as a free-radical initiator and under LED (380–385 nm) irradiation and metal-free conditions, the reaction of alkynoates underwen

Selectivity Controlled Palladium-Catalyzed Carbonylative Synthesis of Propiolates and Chromenones from Phenols and Alkynes

Zhu, Fengxiang,Wu, Xiao-Feng

supporting information, p. 3422 - 3425 (2018/06/11)

An interesting selectivity-controlled palladium-catalyzed oxidative carbonylation procedure for the synthesis of propiolates and chromenones has been developed. Starting from phenols and alkynes, under slightly different conditions, various propiolates an

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