Glycinamide

HCID 69020CAS 1668-10-6

Basic information

Standard SMILES
NCC(N)=O
InChIKey
BEBCJVAWIBVWNZ-UHFFFAOYSA-N
Molecular formula
C2H6N2O
Average molar mass
74.08 g/mol
Monoisotopic mass
74.04801281

Overview

Glycinamide is an amino acid amide and a glycine derivative.

Names & identifiers

Preferred name
Glycinamide
IUPAC
2-aminoacetamide
English name
Glycinamide hydrochloride
Molecular formula
C2H7ClN2O
Molecular weight
110.54

Names & synonyms

Glycinamide2-Aminoacetamide598-41-4Glycine amideAcetamide, 2-amino-AMINOMETHYLAMIDE4JDT453NWODTXSID1060508CHEBI:42843RefChem:663618DTXCID4042701209-932-4
Show more names
2-AMINOACETAMIDE HYDROCHLORIDEGLYCINAMIDE HCLGLYCINE AMIDE HYDROCHLORIDEAminoacetamide hydrochlorideGly-Nh2.HclGLYCINAMIDE HCIGly-NH2.HCIH-GLY-NH2 HCLGLYCINE-NH2 HCLGlycineamide HCl
GLYCINAMIDPiracetam Impurity 112-Amino-AcetamideMFCD018597152-Aminoacetimidic acid4463-18-7aminoacetamideUNII-4JDT453NWO

Database identifiers

CAS
1668-10-6、598-41-4
PubChem CID
69020
DTXSID
DTXSID1060508
ChEMBL
CHEMBL86954
ChEBI
CHEBI:42843
UNII
4JDT453NWO
EC Number
209-932-4
Nikkaji
J2.716B

Properties

Computed structural properties

XLogP
-1.8
Topological polar surface area
69.1 Ų
Hydrogen bond donors
2
Hydrogen bond acceptors
2
Rotatable bonds
1
Heavy atoms
5

Experimental & physicochemical properties

DrugsPharmaceuticals -> Listed in ZINC15
SpringerMaterials PropertiesChemical shift

Physicochemical properties

Melting point
204 °C · 204 °C (dec.)(lit.)
storage temp.
Inert atmosphere,Room Temperature
solubility
2 O: · H2O: 0.1 g/mL, clear
form
Crystalline Powder
color
White to beige
pka
8.2 · 8.20(at 20℃)

Safety & regulation

Safety data

F
3-10
PPE
Eyeshields, Gloves, type N95 (US)
wgk
3
hs_code
29241900
risk_code
36/37/38
Signal word
Warning

Chemistry & industry

Uses & manufacturing

General Manufacturing InformationAcetamide, 2-amino-: INACTIVE
Applications · 2 items

UsesGlycinamide hydrochloride is a buffer that is useful in the physiological pH range. And it is also used as a pharmaceutical intermediate, in the organic synthesis.

UsesGlycinamide hydrochloride may be used in the synthesis of [M(glycinamidato-N,N′)(ptpy)2] where ptpy = 2-(p-tolyl)pyridinato) and M= Rh or Ir. It may be used in the synthesis of the following glycinamide-based imidazolidinones:(±)-2-(2-phenylpropyl)imidazolidin-4-one(±)-2-(2,4,4-trimethylpentyl)imidazolidin-4-one (±)-2-[(R)-2,6-dimethyl-5-heptenyl]imidazolidin-4-one (5R,6S,9R)-6-isopropyl-9-methyl-1,4-diazaspiro[4.5]decan-2-one(5S,6S,9R)-6-isopropyl-9-methyl-1,4-diazaspiro[4.5]decan-2-one(±)-2-methyl-2-pentylimidazolidin-4-one(±)-2-ethyl-2-(2-methylbutyl)imidazolidin-4-one (±)-2-(undecan-2-yl)imidazolidin-4-one (±)-2-pentylimidazolidin-4-one 2-(2,4-dimethylcyclohex-3-en-1-yl)imidazolidin-4-one

Upstream & downstream products

Suppliers50 total

国药集团化学试剂有限公司86-21-63210123 · [email protected]
北京华美互利生物化工010-56205725 · [email protected]
梯希爱(上海)化成工业发展有限公司021-67121386 · [email protected]
衢州润东化工有限公司0570-8789886 18892685668 · [email protected]
上海阿拉丁生化科技股份有限公司400-6206333 13167063860 · [email protected]

Related reactions

132 records

Linked notes

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