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Molecule
ID:131503
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₉H₁₁Cl₂NO₃
Molecular Mass
252.09454
Exact Mass
251.01159858
Charge
0
InChI
InChI=1S/C9H10ClNO3.ClH/c10-6-3-5(1-2-8(6)12)4-7(11)9(13)14;/h1-3,7,12H,4,11H2,(H,13,14);1H
InChIKey
DDKBCJANROGKFJ-UHFFFAOYSA-N
Canonic Smiles
OC(=O)C(Cc1ccc(c(c1)Cl)O)N.Cl
Isomeric Smiles
c1cc(c(cc1CC(C(=O)O)N)Cl)O.Cl
Calculated Properties
JChem
Acid pKa
1.5613557
H Acceptors
4
H Donor
3
LogD (pH = 5.5)
-0.88605565
LogD (pH = 7.4)
-0.99810785
Log P
-0.8850358
Molar Refractivity
51.902
Polarizability
20.454786
Polar Surface Area
83.55
Rotatable Bonds
3
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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Bioactivity
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IUPAC name
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Data Source
Commercial Catalog
Sigma Aldrich
C5897
Academic Data
PubChem
16219143
Names and Identifiers
Synonyms
3-氯-L-酪氨酸 盐酸盐
3-Chloro-L-tyrosine hydrochloride
IUPAC Traditional name
monochlorotyrosine hydrochloride
IUPAC name
2-amino-3-(3-chloro-4-hydroxyphenyl)propanoic acid hydrochloride
Registration numbers
CAS Number
35608-63-0
MDL Number
MFCD00038970
PubChem SID
24892818
162225781
PubChem CID
16219143
Properties
Safety Information
Safety Statements
7
-
24
-
45
Source
GHS Hazard statements
H302
-
H315
-
H319
-
H332
Source
GHS Signal Word
Warning
Source
GHS Precautionary statements
P305+P351+P338
Source
European Hazard Symbols
Harmful (Xn)
Source
Risk Statements
20/22
-
36/38
Source
Storage Temperature
-20°C
Source
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
Source
German water hazard class
3
Source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Source
Product Information
Purity
≥95%
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay