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Molecule
ID:102270
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₀H₁₃NO₂S
Molecular Mass
211.28072
Exact Mass
211.06669966
Charge
0
InChI
InChI=1S/C10H13NO2S/c11-9(10(12)13)7-14-6-8-4-2-1-3-5-8/h1-5,9H,6-7,11H2,(H,12,13)/t9-/m0/s1
InChIKey
GHBAYRBVXCRIHT-VIFPVBQESA-N
Canonic Smiles
N[C@H](C(=O)O)CSCc1ccccc1
Isomeric Smiles
N[C@@H](CSCc1ccccc1)C(=O)O
Calculated Properties
JChem
Acid pKa
2.4173224
H Acceptors
3
H Donor
2
LogD (pH = 5.5)
-0.7841049
LogD (pH = 7.4)
-0.7911801
Log P
-0.7841061
Molar Refractivity
57.5364
Polarizability
22.791697
Polar Surface Area
63.32
Rotatable Bonds
5
Lipinski's Rule of Five
true
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Related Proteins
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Molecular Spectra
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Molecule Details
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General Information
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Bioactivity
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Data Source
Commercial Catalog
MP Biomedicals
02100911
05205263
Sigma Aldrich
B19800
13310
Alfa Aesar
L11666
Bide Pharmatech
BD105969
Academic Data
PubChem
193613
Names and Identifiers
Synonyms
S-BENZYL-L-CYSTEINE
S-苄基-L-半胱氨酸
S-Benzyl-L-cysteine
H-Cys(Bzl)-OH
IUPAC Traditional name
benzylcysteine
IUPAC name
(2R)-2-amino-3-(benzylsulfanyl)propanoic acid
Registration numbers
CAS Number
3054-01-1
EC Number
221-273-4
PubChem SID
162088063
24891622
PubChem CID
193613
Beilstein Number
1879358
MDL Number
MFCD00002613
Molecule Details
MP Biomedicals
02100911
Crystalline
05205263
MP Biomedicals Rare Chemical collection
Sigma Aldrich
B19800
Packaging
10 g in poly bottle
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Registration numbers
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CAS Number
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EC Number
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PubChem SID
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PubChem CID
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Beilstein Number
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MDL Number
Properties
Safety Information
MSDS Link
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Storage Condition
Room Temperature (15-30°C)
Source
German water hazard class
3
Source
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
TSCA Listed
是
Source
Product Information
Certificate of Analysis
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Source
Purity
97%
Source
≥98.0% (NT)
Source
98%
Source
99%
Source
C6H5CH2SCH2CH(NH2)CO2H
Source
purum
Source
Physical Property
Melting Point
214 °C (dec.)(lit.)
Source
~220 °C (dec.)
Source
ca 214°C dec.
Source
Optical Rotation
[α]20/D +23°, c = 2 in 1 M NaOH
Source
[α]20/D +28.5±1°, c = 1.5% in 1 M NaOH
Source
+28 (c=1.5 in 1N NaOH)
Source
Linear Formula
Grade