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18197-22-3

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18197-22-3 Usage

General Description

Iminoaldehyde is a chemical compound also known as an imidoaldehyde. It is a derivative of aldehyde and contains an imine group. Iminoaldehydes are an important class of organic compounds with various applications in organic synthesis. They can be used as intermediates in the production of pharmaceuticals, agrochemicals, and other specialty chemicals. Iminoaldehydes are also used in the development of new materials and as building blocks for the synthesis of other organic molecules. They are known for their reactivity and versatility, making them valuable tools for chemical research and industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 18197-22-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,1,9 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 18197-22:
(7*1)+(6*8)+(5*1)+(4*9)+(3*7)+(2*2)+(1*2)=123
123 % 10 = 3
So 18197-22-3 is a valid CAS Registry Number.
InChI:InChI=1/C2H3NO2/c4-1-3-2-5/h1-2H,(H,3,4,5)

18197-22-3SDS

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 N-formylformamide

1.2 Other means of identification

Product number -
Other names secondary carboxamide

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:18197-22-3 SDS

18197-22-3Relevant articles and documents

Nonracemizable isocyanoacetates for multicomponent reactions

Zhdanko, Alexander G.,Nenajdenko, Valentine G.

supporting information; experimental part, p. 884 - 887 (2009/07/04)

Chiral ortho esters of α-isocyano acids were synthesized from commercially available Cbz-protected α-amino acids. These compounds are stable toward racemization in the Ugi 4CC in contrast to known esters of α-isocyano acids. Applying them in Ugi 4CC with subsequent deprotection gives access to dipeptides with preserved configuration at the C-terminal amino acid.

Use of organophosphorous compounds for producing a medicament for treating infections

-

, (2008/06/13)

The invention relates to the use of organophosphorus compounds of the general formula (I) wherein B is selected from the group which consists of group and group R1—N═A—??(III) and wherein A is selected from the group which consists of an alkyle

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