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1201-90-7

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1201-90-7 Usage

Description

Ethyl 4-chloromethylbenzoate is a chemical substance with a molecular weight of 224.68 g/mol and a molecular formula of C11H11ClO2. It is also known under the CAS number 65816-20-8. Ethyl 4-chloromethylbenzoate is primarily used in the field of organic synthesis, often serving as a synthetic intermediate in the production of other chemical substances.

Uses

Used in Organic Synthesis:
Ethyl 4-chloromethylbenzoate is used as a synthetic intermediate for the production of various chemical substances. Its unique structure allows it to be a valuable component in the synthesis of a wide range of compounds, contributing to the development of new materials and products in the chemical industry.
Used in Chemical Production:
Ethyl 4-chloromethylbenzoate is used as a key component in the manufacturing process of certain chemicals. Its presence in the synthesis process can lead to the creation of new compounds with specific properties, making it an essential part of the chemical production workflow.
Safety and Storage:
Due to limited information available on the potential hazards or safety concerns associated with Ethyl 4-chloromethylbenzoate, it is recommended to handle this compound with the usual precautions for dealing with chemicals. It should be stored in a cool and ventilated area, away from sources of heat or ignition, to minimize the risk of accidents or adverse reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 1201-90-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,0 and 1 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1201-90:
(6*1)+(5*2)+(4*0)+(3*1)+(2*9)+(1*0)=37
37 % 10 = 7
So 1201-90-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H11ClO2/c1-2-13-10(12)9-5-3-8(7-11)4-6-9/h3-6H,2,7H2,1H3

1201-90-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 4-chloromethylbenzoate

1.2 Other means of identification

Product number -
Other names ethyl 4-(chloromethyl)benzoate

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:1201-90-7 SDS

1201-90-7Relevant articles and documents

1,3-dipolar compound bearing an imidazole functional group

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Page/Page column 21-22, (2019/02/20)

In a 1,3-dipolar compound of formula Q-A-B, Q comprises a dipole containing at least and preferably one nitrogen atom, A, which is preferably divalent, is an atom or a group of atoms connecting Q to B, and B comprises an imidazole ring. An unsaturated polymer modified by grafting the 1,3-dipolar compound is also disclosed.

Large-scale preparation of polyfunctional benzylic zinc reagents by direct insertion of zinc dust into benzylic chlorides in the presence of lithium chloride

Metzger, Albrecht,Argyo, Christian,Knochel, Paul

experimental part, p. 882 - 891 (2010/10/01)

Highly functionalized benzylic zinc chlorides are prepared by the direct insertion of commercially available zinc dust into the corresponding benzylic chlorides in the presence of stoichiometric amount of lithium chloride. These polyfunctional zinc organometallics react with various electrophiles leading to a broad range of functionalized products. Georg Thieme Verlag Stuttgart.

High-performance organic semiconductors for thin-film transistors based on 2,7-divinyl[1]benzothieno[3,2-b]benzothiophene

Um, Myoung-Chul,Kwak, Jeonghun,Hong, Jung-Pyo,Kang, Jihoon,Yoon, Do Yeung,Lee, Seong Hoon,Lee, Changhee,Hong, Jong-In

scheme or table, p. 4698 - 4703 (2010/03/24)

We have synthesized two novel organic semiconductors, which have a symmetrically substituted 2,7-divinyl[1]benzothieno[3,2-b]benzothiophene backbone. They show good electrical performances on a SiO2/Si substrate, with high field-effect mobiliti

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