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Merck
CN

73489

Sigma-Aldrich

L-α-新戊基甘氨酸

≥98.0% (TLC)

别名:

γ-甲基-L-亮氨酸, (S)-2-氨基-4,4-二甲基戊酸, L-γ-甲基亮氨酸

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About This Item

经验公式(希尔记法):
C7H15NO2
CAS号:
分子量:
145.20
MDL编号:
UNSPSC代码:
12352209
PubChem化学物质编号:
NACRES:
NA.22

质量水平

方案

≥98.0% (TLC)

表单

solid

反应适用性

reaction type: solution phase peptide synthesis

应用

peptide synthesis

SMILES字符串

[H][C@](N)(CC(C)(C)C)C(O)=O

InChI

1S/C7H15NO2/c1-7(2,3)4-5(8)6(9)10/h5H,4,8H2,1-3H3,(H,9,10)/t5-/m0/s1

InChI key

LPBSHGLDBQBSPI-YFKPBYRVSA-N

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储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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J L Fauchère et al.
International journal of peptide and protein research, 18(3), 249-255 (1981-09-01)
The modified Strecker synthesis of Patel & Worsley was combined with an enzymatic deamidation in the final step, to produce the title compound. The amino acid is a member of the family of the "fat" amino-acids with high lipophilicity and
Xuejing Yu et al.
The FEBS journal, 281(1), 391-400 (2013-11-12)
Branched-chain amino acid aminotransferase (BCAT) plays a key role in the biosynthesis of hydrophobic amino acids (such as leucine, isoleucine and valine), and its substrate spectrum has not been fully explored or exploited owing to the inescapable restrictions of previous

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