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465194

Sigma-Aldrich

Methyl-2-chlorbenzoat

≥98%

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About This Item

Lineare Formel:
ClC6H4CO2CH3
CAS-Nummer:
610-96-8
Molekulargewicht:
170.59
EG-Nummer:
210-242-0
MDL-Nummer:
MFCD00016337
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24870253
NACRES:
NA.22

Assay

≥98%

Form

liquid

Brechungsindex

n20/D 1.536 (lit.)

bp

86-88 °C/2.5 mmHg (lit.)

Dichte

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

InChIKey

JAVRNIFMYIJXIE-UHFFFAOYSA-N

Allgemeine Beschreibung

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.

Anwendung

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.

Lagerklassenschlüssel

10 - Combustible liquids

WGK

WGK 3

Flammpunkt (°F)

228.2 °F - closed cup

Flammpunkt (°C)

109.00 °C - closed cup

Persönliche Schutzausrüstung

Eyeshields, Gloves

Analysenzertifikate (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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