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102266-69-3

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102266-69-3 Usage

General Description

2-[amino(2-oxo-2H-chromen-3-yl)methylene]malononitrile is a chemical compound with the molecular formula C12H6N4O2. It is a yellow solid that is used in organic synthesis and as a precursor for making various pharmaceuticals and organic compounds. The compound contains a malononitrile group and a 2-oxo-2H-chromen-3-yl group, and it has potential biological activities. It can also be used as a ligand in coordination chemistry and as a reagent in organic reactions. Due to its versatile properties, 2-[amino(2-oxo-2H-chromen-3-yl)methylene]malononitrile has various potential industrial and research applications.

Check Digit Verification of cas no

The CAS Registry Mumber 102266-69-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,2,6 and 6 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 102266-69:
(8*1)+(7*0)+(6*2)+(5*2)+(4*6)+(3*6)+(2*6)+(1*9)=93
93 % 10 = 3
So 102266-69-3 is a valid CAS Registry Number.

102266-69-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name <(Amino)(2-oxo-2H-1-benzopyran-3-yl)methylen>malononitril

1.2 Other means of identification

Product number -
Other names 3-amino-2-cyano-3-(2-oxo-2H-1-benzopyran-3-yl)prop-2-enenitrile

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:102266-69-3 SDS

102266-69-3Downstream Products

102266-69-3Relevant articles and documents

Synthetic Reactions of Methyl 2-(2-Amino-3-methoxycarbonyl-4H-1-benzopyran-4-yl)-2-cyanoethanoate

O'Callaghan, Conor N.,McMurry, T. Brian H.

, p. 1448 - 1465 (2007/10/02)

The title ester characteristically undergoes reactions in which the original 4-substituent is displaced, affording a benzopyran fragment which undergoes addition to reactive compounds at either the 4- or the 2-position.Subsequent rearrangement leads to fo

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