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Merck
모든 사진(2)

주요 문서

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284491

Sigma-Aldrich

(R)-(+)-2-Amino-3-phenyl-1-propanol

98%

동의어(들):

D-Phenylalaninol

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모든 사진(2)

About This Item

Linear Formula:
C6H5CH2CH(NH2)CH2OH
CAS Number:
5267-64-1
Molecular Weight:
151.21
Beilstein:
2208239
EC Number:
226-086-1
MDL number:
MFCD00064298
UNSPSC 코드:
12352116
PubChem Substance ID:
24857160
NACRES:
NA.22

분석

98%

형태

solid

광학 활성

[α]/D +22.8°, c = 1.2 in 1 M HCl

mp

93-95 °C (lit.)

작용기

amine
hydroxyl
phenyl

SMILES string

N[C@@H](CO)Cc1ccccc1

InChI

1S/C9H13NO/c10-9(7-11)6-8-4-2-1-3-5-8/h1-5,9,11H,6-7,10H2/t9-/m1/s1

InChI key

STVVMTBJNDTZBF-SECBINFHSA-N

픽토그램

Corrosion
GHS05

신호어

Danger

유해 및 위험 성명서

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

가장 최신 버전 중 하나를 선택하세요:

시험 성적서(COA)

Lot/Batch Number
SHBN0249
SHBF1731V
SHBD7181V
67896APV
67896AP

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L-tert-Leucinol 98%

Sigma-Aldrich

407739

L-tert-Leucinol

(S)-4-Benzyl-2-oxazolidinone 99%

Sigma-Aldrich

294640

(S)-4-Benzyl-2-oxazolidinone

M O Blondel et al.
Biochemical and biophysical research communications, 150(3), 979-986 (1988-02-15)
The illumination of Escherichia coli cells with UVA light, 320 nm less than or equal to lambda less than or equal to 380 nm, triggers a transient growth and division delay. The built-in 4-thiouridine chromophore which absorbs light at 340
W W Mak et al.
Canadian journal of biochemistry, 58(9), 737-744 (1980-09-01)
This study describes a rounding reaction induced in mammalian cells by the addition of phenylalaninol. In the Chinese hamster ovary tsH1 line the rounding occurred rapidly with a half time of 1 min at 25 mM phenylalaninol. After the removal
Violetta Constantinou-Kokotou et al.
Journal of peptide science : an official publication of the European Peptide Society, 11(7), 431-435 (2005-01-07)
2-Oxoamides based on long chain beta-amino acids were synthesized. 1-Benzyl substituted long chain amines, needed for such synthesis, were synthesized starting from Boc-phenylalaninol. The oxidative conversion of a phenyl group to a carboxyl group was used as the key transformation
B Weiss et al.
Research communications in chemical pathology and pharmacology, 62(1), 113-123 (1988-10-01)
An amino acid derivative, leucinethiol, was reported to be a strong inhibitor of aminopeptidase activity. In order to obtain selective inhibitors of various brain aminopeptidases, we tested the inhibition by amino acid analogs of brain aminopeptidase activity. In particular, we
H Hashizume et al.
Chemical & pharmaceutical bulletin, 40(11), 3113-3114 (1992-11-01)
The effects of phenylalaninol (D-isomer) on gastric acid secretion and gastric ulcer were studied in rats. The compound reduced the gastric acid secretion stimulated by intracisternal thyrotropin releasing hormone and intravenous 2-deoxy-D-glucose, but not that stimulated by subcutaneous carbachol or
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