33562
N,N′-二苯甲酰基-L-胱氨酸
98%
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关于此项目
经验公式（希尔记法）:
C20H20N2O6S2
化学文摘社编号:
分子量:
448.51
UNSPSC Code:
12352209
NACRES:
NA.22
PubChem Substance ID:
EC Number:
246-640-6
Beilstein/REAXYS Number:
2068210
MDL number:
InChI key
GUTXMPQWQSOAIY-HOTGVXAUSA-N
InChI
1S/C20H20N2O6S2/c23-17(13-7-3-1-4-8-13)21-15(19(25)26)11-29-30-12-16(20(27)28)22-18(24)14-9-5-2-6-10-14/h1-10,15-16H,11-12H2,(H,21,23)(H,22,24)(H,25,26)(H,27,28)/t15-,16-/m0/s1
SMILES string
OC(=O)[C@H](CSSC[C@H](NC(=O)c1ccccc1)C(O)=O)NC(=O)c2ccccc2
assay
98%
form
powder
optical activity
[α]20/D −215±8°, c = 1% in ethanol
reaction suitability
reaction type: solution phase peptide synthesis
mp
195-200 °C (dec.)
application(s)
peptide synthesis
Quality Level
Application
Reactant involved in:
- Synthesis of integrin antagonists
- Dissipative self-assembly of molecular gelator using chemical fuel
- Synthesis of crosslinkable hydrogel for proliferation of encapsulated human derm fibroblast
- Analysis for use as metallo-β-lactamase inhibitors
- Amplification of bifunctional disulfide ligands for calmodulin
Other Notes
LiBH4 手性修饰剂，用于芳香族、杂芳族和不饱和酮不对称还原为醇
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Journal of the Chemical Society. Chemical Communications, 138-138 (1985)
P.G. Sammes et al.
Journal of the Chemical Society. Perkin Transactions 1, 111-111 (1988)
K. Soai et al.
Journal of the Chemical Society. Chemical Communications, 413-413 (1984)
Journal of the Chemical Society. Chemical Communications, 801-801 (1987)
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