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Merck
CN

T3629

Sigma-Aldrich

DL-间酪氨酸

≥98% (HPLC)

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别名:
(±)-2-氨基-3-(3-羟基苯基)丙酸, 3-(3-羟基苯基)-DL-丙氨酸
线性分子式:
HOC6H4CH2CH(NH2)CO2H
CAS号:
分子量:
181.19
Beilstein:
2416853
EC 号:
MDL编号:
UNSPSC代码:
12352209
PubChem化学物质编号:
NACRES:
NA.26

检测方案

≥98% (HPLC)

质量水平

形式

crystalline

颜色

off-white to yellow

mp

280-285 °C (dec.) (lit.)

溶解性

1 M HCl: soluble

应用

detection

SMILES字符串

NC(Cc1cccc(O)c1)C(O)=O

InChI

1S/C9H11NO3/c10-8(9(12)13)5-6-2-1-3-7(11)4-6/h1-4,8,11H,5,10H2,(H,12,13)

InChI key

JZKXXXDKRQWDET-UHFFFAOYSA-N

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象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

WGK

WGK 3

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves


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P Manini et al.
The Journal of organic chemistry, 66(15), 5048-5053 (2001-07-21)
In 0.1 M phosphate buffer at pH 7.4 and 37 degrees C, the tyrosine metabolite L-3,4-dihydroxyphenylalanine (L-DOPA) reacts smoothly with D-glucose to afford, besides diastereoisomeric tetrahydroisoquinolines 1 and 2 by Pictet-Spengler condensation, a main product shown to be the unexpected
Catecholamines and dihydroxyphenylalanine in metamorphosing larvae of the nudibranch Phestilla sibogae Bergh (Gastropoda: Opisthobranchia).
Pires A, Coon SL, Hadfield MG.
J. Comp. Physiol., 181, 187-194 (1997)
A Pappa-Louisi et al.
Methods in molecular biology (Clifton, N.J.), 828, 101-114 (2011-11-30)
The combined use of a dual-UV detector as well as a fluorimetric and a multielectrode electrochemical detector (equipped with a dual electrode, consisting of a conventional size 3 mm diameter glassy carbon electrode (GCE) and of a pair of 30
Harleen Kaur et al.
PloS one, 4(3), e4700-e4700 (2009-03-12)
Allelopathy (negative, plant-plant chemical interactions) has been largely studied as an autecological process, often assuming simplistic associations between pairs of isolated species. The growth inhibition of a species in filter paper bioassay enriched with a single chemical is commonly interpreted
Regioselective asymmetric aminohydroxylation approach to a beta-hydroxyphenylalanine derivative for the synthesis of ustiloxin D.
H Park et al.
The Journal of organic chemistry, 66(21), 7223-7226 (2001-10-13)

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