检测方案
≥98%
形式
liquid
折射率
n20/D 1.536 (lit.)
bp
86-88 °C/2.5 mmHg (lit.)
密度
1.191 g/mL at 25 °C (lit.)
SMILES字符串
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
一般描述
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.
应用
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.
WGK
WGK 3
闪点(°F)
228.2 °F
闪点(°C)
109.00 °C
个人防护装备
Eyeshields, Gloves
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.
Synthetic Communications, 33(10), 1733-1750 (2003)
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
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
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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