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1-(Chloromethyl)-4-(cyclopropylmethoxy)benzene is an organic chemical compound characterized by its molecular formula C10H11ClO. It is a benzene derivative featuring a chloromethyl group and a cyclopropylmethoxy group attached to the benzene ring. 1-(chloromethyl)-4-(cyclopropylmethoxy)benzene is known for its potential applications in various industries, particularly due to its chemical reactivity and unique structural features.

183994-41-4

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183994-41-4 Usage

Uses

Used in Pharmaceutical Industry:
1-(Chloromethyl)-4-(cyclopropylmethoxy)benzene is used as an intermediate in the synthesis of other organic compounds for the pharmaceutical industry. Its unique structure allows for the creation of a wide range of pharmaceutical products, contributing to the development of new medications and therapies.
Used in Agrochemical Industry:
Similarly, in the agrochemical industry, 1-(chloromethyl)-4-(cyclopropylmethoxy)benzene serves as an intermediate in the synthesis of various organic compounds. Its application in this field aids in the production of chemicals used for agricultural purposes, such as pesticides and fertilizers, enhancing crop protection and yield.
Used as a Substrate for Enzymatic Reactions:
1-(Chloromethyl)-4-(cyclopropylmethoxy)benzene is also a potential substrate for enzymatic reactions. This characteristic opens up possibilities for its use in research and development, particularly in the field of biochemistry and molecular biology, where it can be employed to study enzyme specificity and catalytic mechanisms.
Biological Activity:
Due to its chemical structure, 1-(chloromethyl)-4-(cyclopropylmethoxy)benzene may possess biological activity, which could be harnessed for various applications in the life sciences. Further research and development are necessary to fully understand and exploit its potential in this area.
Safety Precautions:
Given its chemical reactivity and potential health hazards, 1-(chloromethyl)-4-(cyclopropylmethoxy)benzene should be handled and used with proper safety measures. This includes adhering to guidelines for chemical handling, using appropriate personal protective equipment, and ensuring proper disposal and storage methods to minimize risks.

Check Digit Verification of cas no

The CAS Registry Mumber 183994-41-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,3,9,9 and 4 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 183994-41:
(8*1)+(7*8)+(6*3)+(5*9)+(4*9)+(3*4)+(2*4)+(1*1)=184
184 % 10 = 4
So 183994-41-4 is a valid CAS Registry Number.

183994-41-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(chloromethyl)-4-(cyclopropylmethoxy)benzene

1.2 Other means of identification

Product number -
Other names -

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:183994-41-4 SDS

183994-41-4Relevant academic research and scientific papers

Cyclopropylmethyl Protection of Phenols: Total Synthesis of the Resveratrol Dimers Anigopreissin A and Resveratrol–Piceatannol Hybrid

Kumar, Arvind,Saleeb, Michael,Werz, Dominik,Elofsson, Mikael

, p. 953 - 956 (2018/11/23)

We demonstrate the versatile use of the cyclopropylmethyl group to protect phenols through the total synthesis of two benzofuran-based natural products, that is, anigopreissin A and the resveratrol–piceatannol hybrid. This protecting group is a good alter

Total synthesis of the resveratrol oligomers (±)-Ampelopsin B and (±)-σ-Viniferin

Lindgren, Anders E. G.,?berg, Christopher T.,Hillgren, J. Mikael,Elofsson, Mikael

, p. 426 - 429 (2016/02/18)

The total synthesis of the resveratrol dimers (±)-ampelopsin B and (±)-σ-viniferin is reported. Highlights of the approach include the use of cyclopropylmethyl groups to protect aromatic alcohols. This group allows an acid promoted three-step, one-pot dep

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