270792
4-(Chloromethyl)benzoic acid
95%
Synonym(s):
α-Chloro-p-toluic acid, α-Chloro-p-toluylic acid
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About This Item
Empirical Formula (Hill Notation):
C8H7ClO2
CAS Number:
Molecular Weight:
170.59
Beilstein:
1907970
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
95%
form
powder
mp
201-202 °C (lit.)
functional group
carboxylic acid
SMILES string
OC(=O)c1ccc(CCl)cc1
InChI
1S/C8H7ClO2/c9-5-6-1-3-7(4-2-6)8(10)11/h1-4H,5H2,(H,10,11)
InChI key
OITNBJHJJGMFBN-UHFFFAOYSA-N
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Related Categories
Application
4-(Chloromethyl)benzoic acid was used in the synthesis of dihydroxy stilbene derivatives.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1 - Resp. Sens. 1 - Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Polysulfone (PSf) membrane is widely employed in blood purification fields, but the blood compatibility of PSf membrane is not adequate. To improve the hemocompatibility of PSf membrane, 4-(chloromethyl)benzoic acid (CMBA) and sulfonated hydroxypropyl chitosan (SHPCS) were grafted onto PSf membrane
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Bioorganic & medicinal chemistry letters, 17(16), 4481-4486 (2007-06-29)
Dihydroxy stilbene derivatives were designed based on lithospermic acid B and were prepared from 4-(chloromethyl)benzoic acid. The inhibitory activities of the novel compounds against protein tyrosine phosphatase 1B (PTP1B) were evaluated. 3,4-Dihydroxy stilbene carbonyl compounds (7, 11b, 27b) inhibited PTP1B
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In this work, the anodic current at an electrode grafted with a molecularly imprinted polymer (MIP) crosslinked via a combination of hydrophobic ethyleneglycol dimethacrylate (EDMA) and hydrophilic methylene bisacrylamide (MBAA) was found to exhibit enantioselective sensitivity to the phenylalanine template
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