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About This Item
Linear Formula:
ClC6H4CO2CH3
CAS Number:
Molecular Weight:
170.59
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
≥98%
form
liquid
refractive index
n20/D 1.536 (lit.)
bp
86-88 °C/2.5 mmHg (lit.)
density
1.191 g/mL at 25 °C (lit.)
SMILES string
COC(=O)c1ccccc1Cl
InChI
1S/C8H7ClO2/c1-11-8(10)6-4-2-3-5-7(6)9/h2-5H,1H3
InChI key
JAVRNIFMYIJXIE-UHFFFAOYSA-N
General description
Methyl 2-chlorobenzoate, a methyl 2-halobenzoate, is an ester. It can be synthesized from 2-chlorobenzoyl chloride. Its reduction with NaBH4 in diglyme at 162°C affords 2-chlorobenzyl alcohol.
Application
Methyl 2-chlorobenzoate may be used in the synthesis of various quinazolinone derivatives. It was used as starting reagent in the synthesis of 2-chlorobenzohydrazide.
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
228.2 °F - closed cup
Flash Point(C)
109.00 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Navin B Patel et al.
Scientia pharmaceutica, 78(2), 171-193 (2010-12-24)
In attempt to find new pharmacologically active molecules, we report here the synthesis and in vitro antimicrobial activity of various 3-(1,3,4-oxadiazol-2-yl)-quinazolin-4(3H)-ones. The antimicrobial activity of title compounds were examined against two gram positive bacteria (S. aureus, S. pyogenes), two gram
Reductions of Carboxylic Acids and Esters with NaBH4 in Diglyme at 162?C.
Zhu H-J and Pittman Jr CU.
Synthetic Communications, 33(10), 1733-1750 (2003)
Cheng Huang et al.
Chemical communications (Cambridge, England), (47)(47), 6333-6335 (2008-12-03)
We have developed a general and highly efficient copper-catalyzed method for synthesis of quinazoline and quinazolinone derivatives, the target products were obtained in good to excellent yields via cascade reactions of amidine hydrochlorides with substituted 2-halobenzaldehydes, 2-halophenylketones, or methyl 2-halobenzoates
Nicholas R Larson et al.
Journal of medical entomology, 57(1), 187-191 (2019-09-10)
Common bed bug Cimex lectularius (L.) (Hemiptera: Cimicidae) infestations are on the rise and due to the development of pesticide resistance they are becoming more difficult to control, affordably. We evaluated a naturally occurring compound methyl benzoate (MB) and related
Yan Feng et al.
Scientific reports, 8(1), 7902-7902 (2018-05-23)
Benzyl methyl ester, also known as methyl benzoate (MB), is a volatile organic compound that exists naturally as a floral fragrance in many plants. Our behavioral bioassays show that MB and some of its naturally occurring and synthetic analogs kill
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