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经验公式(希尔记法):
C6H11NO3S
化学文摘社编号:
分子量:
177.22
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
32160406
UNSPSC Code:
12352209
MDL number:
Beilstein/REAXYS Number:
1724357
产品名称
N-乙酰基-L-半胱氨酸甲酯, ≥90% (HPLC)
InChI
1S/C6H11NO3S/c1-4(8)7-5(3-11)6(9)10-2/h5,11H,3H2,1-2H3,(H,7,8)/t5-/m0/s1
SMILES string
COC(=O)[C@H](CS)NC(C)=O
InChI key
QTKAQJWFVXPIFV-YFKPBYRVSA-N
assay
≥90% (HPLC)
form
powder or crystals
optical activity
[α]20/D −24.0±3°, c = 1% in methanol
reaction suitability
reaction type: solution phase peptide synthesis
color
white to faint yellow
mp
77-81 °C
application(s)
peptide synthesis
Quality Level
Other Notes
硫转移剂
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)
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Amy E M Beedle et al.
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Mechanical force modifies the free-energy surface of chemical reactions, often enabling thermodynamically unfavoured reaction pathways. Most of our molecular understanding of force-induced reactivity is restricted to the irreversible homolytic scission of covalent bonds and ring-opening in polymer mechanophores. Whether mechanical
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