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836-42-0

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836-42-0 Usage

General Description

4-(Benzyloxy)benzyl chloride is a chemical compound consisting of a benzyl group attached to a benzene ring via an ether linkage, and a chlorine atom attached to the benzyl group. It is a highly reactive compound that is commonly used in organic synthesis as a reagent for various chemical reactions, such as nucleophilic substitution and Friedel-Crafts acylation. It is also used in the production of pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactivity and potential hazards, 4-(Benzyloxy)benzyl chloride should be handled and stored with care, and appropriate safety precautions should be taken when working with this compound.

Check Digit Verification of cas no

The CAS Registry Mumber 836-42-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,3 and 6 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 836-42:
(5*8)+(4*3)+(3*6)+(2*4)+(1*2)=80
80 % 10 = 0
So 836-42-0 is a valid CAS Registry Number.
InChI:InChI=1/C13H11ClO/c14-10-11-6-8-13(9-7-11)15-12-4-2-1-3-5-12/h1-9H,10H2

836-42-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(Benzyloxy)benzyl chloride

1.2 Other means of identification

Product number -
Other names 1-(chloromethyl)-4-phenylmethoxybenzene

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:836-42-0 SDS

836-42-0Relevant articles and documents

Topochemical polymerisation of assembled diacetylene macrocycle bearing dibenzylphosphine oxide in solid state

Zhang, Xiaoning,Deng, Chao,Wang, Meng,Liu, Xin,Lin, Chen,Peng, Luming,Wang, Leyong

, p. 94 - 101 (2017)

Novel diacetylene macrocycles 1 and 2 bearing dibenzylphosphine oxide were synthesised via Eglinton acetylenic intramolecular coupling. The X-ray analysis of crystals of macrocycles 1 and 2 demonstrated that the better-aligned tubular supramolecular structure was formed in macrocycle 1 than in macrocycle 2, which provided the possibility of diacetylene topochemical polymerisation in solid state of macrocycle 1. UV–vis, Raman spectroscopy and X-ray analysis indicated that the crystals of macrocycle 1 could undergo topochemical diacetylene polymerisation only on their surface by light irradiation; differential scanning calorimetry, solid-state 13C NMR spectroscopy and solubility test demonstrated that the crystals of macrocycle 1 could undergo diacetylene topochemical polymerisation inside solid by heat. As expected, based on the topological analysis of crystal structure, the crystals of macrocycle 2 could not undergo diacetylene topochemical polymerisation either by light irradiation or heat.

Fumarate related impurity and preparation method and application thereof (by machine translation)

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Paragraph 0095-0096, (2020/02/04)

The preparation method of the related impurities comprises the following steps: No.No.No. STR8No.No. wherein the (I) preparation method, of ,R the related impurities is. shown, in the specification, and the preparation method of, the 1 present, application, further, discloses, the preparation method, and of the related impurities. (by machine translation)

Benzofuran compound and its preparation, use (by machine translation)

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Paragraph 0063-0064, (2017/08/18)

The invention relates to a benzofuran compound and its preparation, use, its structural formula such as formula (I) as shown: Wherein R1 , R2 , R4 Are selected from hydrogen, C1 - C5 Alkyl, nitro, halogen, ester, hydroxy, amino, amide base or alkoxyl; R3 Hydrogen, C1 - C5 Alkyl, benzyl, aromatic or heteroaromatic group. The invention also relates to the benzofuran compounds in inhibiting the application of gram-positive to be used repeatedly. The invention relates to 3 - oxime substituted benzene and furan structure aromatic ring as the center, the establishment and optimize the preparation method of the compound, and on the preparation of novel compound of the bacteriostatic screening experiment, through initial bacteriostatic test to confirm that preparation compound has broad-spectrum bacteriostatic activity. (by machine translation)

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