18197-22-3

Basic information

• Product Name: IMINOALDEHYDE
• Synonyms: IMINOALDEHYDE
• CAS NO: 18197-22-3
• Molecular Formula: C₂H₃NO₂
• Molecular Weight: 73.0507
• Mol File: 18197-22-3.mol

Chemical Properties

• Melting Point: 41.5°C
• Boiling Point: 128.84°C (rough estimate)
• Flash Point: 68.5°C
• Appearance: /
• Density: 1.3248 (rough estimate)
• Vapor Pressure: 11.8mmHg at 25°C
• Refractive Index: 1.4200 (estimate)
• CAS DataBase Reference: IMINOALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: IMINOALDEHYDE(18197-22-3)
• EPA Substance Registry System: IMINOALDEHYDE(18197-22-3)

Safety Data

• Hazardous Substances Data: 18197-22-3(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
Iminoaldehyde is used as an intermediate in the production of pharmaceuticals for its ability to be used in the synthesis of various drug compounds.
Used in Agrochemical Industry:
Iminoaldehyde is used as an intermediate in the production of agrochemicals for its ability to be used in the synthesis of various agrochemical compounds.
Used in Specialty Chemicals Industry:
Iminoaldehyde is used as an intermediate in the production of specialty chemicals for its ability to be used in the synthesis of various specialty chemical compounds.
Used in Material Development:
Iminoaldehyde is used in the development of new materials for its ability to be used as a building block for the synthesis of other organic molecules.
Used in Organic Synthesis:
Iminoaldehyde is used as a building block for the synthesis of other organic molecules for its reactivity and versatility in organic synthesis.

InChI:InChI=1/C2H3NO2/c4-1-3-2-5/h1-2H,(H,3,4,5)

Upstream product

• 77287-34-4 formamide 
• 288-42-6 oxazol 
• 18197-26-7 sodium diformamide 
• 90801-71-1 N-Formylformamidinium bromide 
• 76085-56-8 N-(dichloromethyl)methanimidamide hydrochloride 

Downstream Products

• 25891-31-0 triformylamine 
• 766-93-8 N-cyclohexylformamide 
• 3760-54-1 1-pyrrolidinecarboxaldehyde 
• 104-62-1 formic acid phenethyl ester 
• 4351-55-7 cholesteryl formate 
• 71921-02-3 2-benzyl-2-formamidoacetic acid methyl ester 
• 3085-54-9 N-(4-methylphenyl)formamide 
• 2617-79-0 N-(4-chlorophenyl)formamide 
• 6343-54-0 N-benzylformamide 
• 104-57-4 benzyl formate 
• 592-84-7 n-butyl formate 
• 120-14-9 3,4-dimethoxy-benzaldehyde 
• 123-11-5 4-methoxy-benzaldehyde 
• 126748-44-5 N-[bis(4-methoxyphenyl)methyl]-formamide 

Relevant articles and documents

Nonracemizable isocyanoacetates for multicomponent reactions

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.

Salts and ionic liquids of resonance stabilized amides

The synthesis, structure, and bonding of alkali salts of resonance stabilized amides, such as diformylamide (dfa), formylcyanoamide (fca), nitrocyanoamide (nca), and for comparision, the well-known dicyanoamide (dca), are discussed on the basis of experim

Use of organophosphorous compounds for producing a medicament for treating infections

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

FORMYLATION REACTION USING THE OZONOLYSATE OF OXAZOLE

The ozonolysis of oxazole (1) did not give formic anhydride (3), but gave N-formylformamide (5), which reacted with various nucleophiles to afford the corresponding formylated products in high yield.This formylating reaction should be useful in the organic syntheses.