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Merck
CN

285463

Sigma-Aldrich

D-胱氨酸

98%, for peptide synthesis

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别名:
(S,S)-3,3′-二硫代双(2-氨基丙酸)
线性分子式:
[-SCH2CH(NH2)CO2H]2
CAS号:
分子量:
240.30
Beilstein:
1728093
EC 号:
MDL编号:
UNSPSC代码:
12352209
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

98%

旋光性

[α]20/D +212°, c = 1 in 1 M HCl

反应适用性

reaction type: solution phase peptide synthesis

mp

265 °C (dec.) (lit.)

应用

peptide synthesis

SMILES字符串

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

InChI

1S/C6H12N2O4S2/c7-3(5(9)10)1-13-14-2-4(8)6(11)12/h3-4H,1-2,7-8H2,(H,9,10)(H,11,12)/t3-,4-/m1/s1

InChI key

LEVWYRKDKASIDU-QWWZWVQMSA-N

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WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)

法规信息

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Masashi Harada et al.
Journal of chromatography. A, 1593, 91-101 (2019-02-12)
Novel sophisticated derivatizing agents for the efficient enantioselective separation and mass spectrometric detection of d- and l-amino acids have been developed. Two new axially chiral reagents derived from 6,6'-dimethyl-2,2'-biphenyldiamine were synthesized. Their chiral separation and detection abilities were evaluated by
Theresa K Tiefenbrunn et al.
Protein science : a publication of the Protein Society, 18(5), 970-979 (2009-04-23)
The type 1 repeat domain from thrombospondin has potent antiangiogenic activity and a structurally interesting fold, making it an attractive target for protein engineering. Chemical synthesis is an attractive approach for studying protein domains because it enables the use of

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