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106012-58-2

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106012-58-2 Usage

General Description

IMIDAZO[1,2-A]PYRAZINE-3-CARBALDEHYDE is a chemical compound with the molecular formula C8H6N2O. It is also known by the synonyms "imidazo[1,2-a]pyrazine-3-carboxaldehyde" and "3-formylimidazo[1,2-a]pyrazine". IMIDAZO[1,2-A]PYRAZINE-3-CARBALDEHYDE is a heterocyclic aldehyde, meaning it contains a ring structure with at least two different elements. It is commonly used in the pharmaceutical industry as a building block for the synthesis of various pharmaceutical compounds. Its unique structure and reactivity make it valuable for the production of drugs and other bioactive molecules. Additionally, IMIDAZO[1,2-A]PYRAZINE-3-CARBALDEHYDE may have potential applications in other fields such as materials science and chemical synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 106012-58-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,0,1 and 2 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 106012-58:
(8*1)+(7*0)+(6*6)+(5*0)+(4*1)+(3*2)+(2*5)+(1*8)=72
72 % 10 = 2
So 106012-58-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H5N3O/c11-5-6-3-9-7-4-8-1-2-10(6)7/h1-5H

106012-58-2SDS

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 IMIDAZO[1,2-A]PYRAZINE-3-CARBALDEHYDE

1.2 Other means of identification

Product number -
Other names -

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

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More Details:106012-58-2 SDS

106012-58-2Downstream Products

106012-58-2Relevant articles and documents

C-3 Hydroxylation of Some Imidazoazines

Teulade, Jean C.,Bonnet, Pierre A.,Rieu, Jean N.,Viols, Henry,Chapat, Jean P.,et al.

, p. 1842 - 1874 (2007/10/02)

Reactions of imidazopyridine, pyrimidine and pyrazine (1)-(3) with formaldehyde or acetaldehyde give the corresponding alcohols and secondary products characterized by 1H and 13C n.m.r.X-Ray crystallographic analysis confirms the structure of (6).The two-step sequence of n-butyllithium and reaction with aldehydes with (2)-(3) does not lead to the alcohols but to n-butyl derivatives with substituents at C(7) and C(8) respectively.

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