추천 제품
Quality Level
분석
≥99.0% (AT)
형태
solid
pKa(20 °C)
8.20
solubility
H2O: 0.1 g/mL, clear, colorless
음이온 미량물
sulfate (SO42-): ≤50 mg/kg
양이온 미량물
Ca: ≤10 mg/kg
Cd: ≤5 mg/kg
Co: ≤5 mg/kg
Cr: ≤5 mg/kg
Cu: ≤5 mg/kg
Fe: ≤5 mg/kg
K: ≤50 mg/kg
Mg: ≤5 mg/kg
Mn: ≤5 mg/kg
Na: ≤50 mg/kg
Ni: ≤5 mg/kg
Pb: ≤5 mg/kg
Zn: ≤5 mg/kg
λ
0.5 M in H2O
UV 흡수
λ: 260 nm Amax: 0.1
작용기
amide
amine
SMILES string
Cl.NCC(N)=O
InChI
1S/C2H6N2O.ClH/c3-1-2(4)5;/h1,3H2,(H2,4,5);1H
InChI key
WKNMKGVLOWGGOU-UHFFFAOYSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
애플리케이션
Glycinamide 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:
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
기타 정보
Use in peptide coupling.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Eyeshields, Gloves, type N95 (US)
Synthesis and Characterization of New Bis-Cyclometalated Rhodium and Iridium Complexes Containing the Glycinamidato Ligand.
Zeitschrift fur Anorganische und Allgemeine Chemie, 639(7), 1117-1121 (2013)
Controlled gelation and sintering of monolithic gels prepared from g-alumina fume powder.
Journal of the American Ceramic Society. American Ceramic Society, 74(4), 830-836 (1991)
Preparation of Imidazolidin-4-ones and Their Evaluation as Hydrolytically Cleavable Precursors for the Slow Release of Bioactive Volatile Carbonyl Derivatives.
European Journal of Organic Chemistry, 2012(14), 2837-2854 (2012)
Journal of the Chemical Society. Perkin Transactions 1, 2299-2299 (1985)
Biochemistry, 46(13), 4037-4044 (2007-03-14)
As a model for mechanistic comparison with peptidyl transfer within the ribosome, the reaction of aqueous glycinamide with N-formylphenylalanine trifluoroethyl ester (fPhe-TFE) represents an improvement over earlier model reactions involving Tris. The acidity of trifluoroethanol (pKa 12.4) resembles that of
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