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4349-62-6

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4349-62-6 Usage

General Description

2-(benzyloxy)benzoyl chloride is a chemical compound with the formula C14H11ClO2. It is a benzoyl chloride derivative containing a benzyloxy group, and is often used as a reagent in chemical reactions for the synthesis of various organic compounds. It is a colorless to pale yellow liquid with a pungent odor, and is highly reactive, especially with water and moisture. It is important to handle 2-(benzyloxy)benzoyl chloride with caution, as it can cause severe skin and eye irritation, and may also be harmful if inhaled or ingested. 2-(benzyloxy)benzoyl chloride is commonly used in the pharmaceutical and agrochemical industries for the production of various drugs and pesticides.

Check Digit Verification of cas no

The CAS Registry Mumber 4349-62-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,4 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4349-62:
(6*4)+(5*3)+(4*4)+(3*9)+(2*6)+(1*2)=96
96 % 10 = 6
So 4349-62-6 is a valid CAS Registry Number.

4349-62-6 Well-known Company Product Price

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  • Aldrich

  • (707597)  2-Benzyloxybenzoylchloride  97%

  • 4349-62-6

  • 707597-5G

  • 2,669.94CNY

  • Detail

4349-62-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenylmethoxybenzoyl chloride

1.2 Other means of identification

Product number -
Other names Benzoyl chloride,2-(phenylmethoxy)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4349-62-6 SDS

4349-62-6Relevant articles and documents

Synthesis and preliminary biological evaluations of 5'-substituted derivatives of uridine as glycosyltransferase inhibitors

Paszkowska, Jadwiga,Kral, Katarzyna,Bieg, Tadeusz,Nawrot, Urszula,Szeja, Wieslaw,Wandzik, Ilona

, p. 8018 - 8027 (2013)

New derivatives of uridine which contain a β-ketoenol motif were synthesized, characterized and biologically tested. Synthesized compounds 1-4 showed no activity against bovine milk β-1,4-galactosyltransferase I at concentrations up to 2.0 mM and were not

Capsaicine derivatives, preparation method of capsaicine derivatives and application of capsaicine derivatives in preparation of drugs for cardiovascular diseases

-

Paragraph 0038-0041, (2020/12/05)

The invention provides capsaicine derivatives, a preparation method of the capsaicine derivatives and an application of the capsaicine derivatives in preparation of drugs for cardiovascular diseases.A compound has a structure as shown in a general formula

Metal-free Synthesis of Spiro-2,2′-benzo[b]furan-3,3′-ones via PhI(OAc)2-Mediated Cascade Spirocyclization

Xing, Qingyu,Liang, Huiyuan,Bao, Mingmai,Li, Xuemin,Zhang, Jingran,Bi, Tianhao,Zhang, Yilin,Xu, Jun,Du, Yunfei,Zhao, Kang

, p. 4669 - 4673 (2019/09/17)

Treating the benzyl protected 3-hydroxy-1,3-bis(2-hydroxyphenyl)prop-2-en-1-ones solely with PhI(OAc)2 (PIDA) in DCE at room temperature readily furnished the seldom studied spiro-2,2′-benzo[b]furan-3,3′-ones in satisfactory to excellent yields. The hypervalent iodine reagent enables the metal-free cascade spirocyclization resulting in the dual oxidative C?O bond formation. (Figure presented.).

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