Detail of "627-95-2"

CAS Number:
627-95-2
Name:
Pentanoic acid,5-amino-, hydrochloride (1:1)
Molecular Structure:
Formula:
C₅H₁₂ClNO₂
Molecular Weight:
153.61
Synonyms:
Pentanoic acid,5-amino-, hydrochloride (9CI);Valeric acid, 5-amino-, hydrochloride (8CI);5-Aminopentanoic acid hydrochloride;5-Aminovaleric acid hydrochloride;d-Aminovaleric acid hydrochloride;
EINECS:
211-021-1
Melting Point:
95-97 °C(lit. )
Boiling Point:
247.5 °C at 760 mmHg
Flash Point:
103.5 °C
Appearance:
light pink crystalline powder
Hazard Symbols:
Xn
Risk Codes:
20/21/22-36/37/38
Safety:
24/25-36-26 Details

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5-AMINOVALERIC ACID HYDROCHLORIDE

Supplier:Hangzhou Share Chemical Co., Ltd [ China (Mainland)]

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5-Aminovaleric Acid Hydrochloride

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Synthesis of 2-amino acids via selective mono-N-alkylation of trichloroacetamide by 2-bromo carboxylic esters under solid-liquid phase-transfer catalysis conditions: Synthesis of 2-amino acids via selective mono-N-alkylation of trichloroacetamide by 2-bromo carboxylic esters under solid-liquid phase-transfer catalysis conditions. Albanese, Domenico; Landini, Dario; Penso, Michele (Dip. Chim. Org. Ind., Univ. Milano, Milan I-20133, Italy).Some commonly used reagents like 600-00-0 is used in this experiment. J. 627-95-2 is also in the experiment. Org. Chem., 57(5), 1603-5 (English) 1992. CODEN: JOCEAH. ISSN: 0022-3263. DOCUMENT TYPE: Journal CA Section: 34 (Amino Acids, Peptides, and Proteins) N-Trichloroacetyl amino acid esters Cl3CCONHCHRCO2R1 (I; R = H, Me, Et, n-C6H13, CH2Ph, R1 = Et; R = n-C14H29, CH2CHMe2, R1 = Me) were prepd. by the selective mono-N-alkylation of Cl3CCONH2 with RCHBrCO2R1 under solid-liq. phase-transfer catalysis conditions. I were hydrolyzed to give amino acids H2NCHRCO2H. ..

Synthesis of 2-amino acids via selective mono-N-alkylation of trichloroacetamide by 2-bromo carboxylic esters under solid-liquid phase-transfer catalysis conditions: Synthesis of 2-amino acids via selective mono-N-alkylation of trichloroacetamide by 2-bromo carboxylic esters under solid-liquid phase-transfer catalysis conditions. Albanese, Domenico; Landini, Dario; Penso, Michele (Dip. Chim. Org. Ind., Univ. Milano, Milan I-20133, Italy).Some commonly used reagents like 600-00-0 is used in this experiment. J. 627-95-2 is also in the experiment. Org. Chem., 57(5), 1603-5 (English) 1992. CODEN: JOCEAH. ISSN: 0022-3263. DOCUMENT TYPE: Journal CA Section: 34 (Amino Acids, Peptides, and Proteins) N-Trichloroacetyl amino acid esters Cl3CCONHCHRCO2R1 (I; R = H, Me, Et, n-C6H13, CH2Ph, R1 = Et; R = n-C14H29, CH2CHMe2, R1 = Me) were prepd. by the selective mono-N-alkylation of Cl3CCONH2 with RCHBrCO2R1 under solid-liq. phase-transfer catalysis conditions. I were hydrolyzed to give amino acids H2NCHRCO2H. ..