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1-[2-[4-(Chloromethyl)phenoxy]ethyl]hexahydro-1H-azepine is a complex chemical compound featuring a hexahydro-1H-azepine core connected to a phenoxyethyl group with a chloromethyl substituent. 1-[2-[4-(Chloromethyl)phenoxy]ethyl]hexahydro-1H-azepine is recognized for its versatility in organic synthesis and drug development due to its reactive chloromethyl group, which facilitates various chemical modifications.

212771-30-7

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212771-30-7 Usage

Uses

Used in Organic Synthesis:
1-[2-[4-(Chloromethyl)phenoxy]ethyl]hexahydro-1H-azepine is used as a building block for the synthesis of other organic compounds. Its unique structure and functionalizable chloromethyl group make it a valuable intermediate in creating a range of chemical products.
Used in Pharmaceutical Drug Development:
In the pharmaceutical industry, 1-[2-[4-(Chloromethyl)phenoxy]ethyl]hexahydro-1H-azepine is utilized as a key component in the development of new drugs. Its reactivity and structural features contribute to the design of innovative therapeutic agents.
Used in Materials Science:
1-[2-[4-(Chloromethyl)phenoxy]ethyl]hexahydro-1H-azepine may also find applications in materials science, where its properties can be harnessed to develop new materials with specific characteristics, such as improved stability or reactivity.
Overall, 1-[2-[4-(Chloromethyl)phenoxy]ethyl]hexahydro-1H-azepine is a multifaceted chemical with potential applications across various industries, primarily due to its structural complexity and the reactivity of its chloromethyl group, which allows for extensive chemical modifications and functionalization.

Check Digit Verification of cas no

The CAS Registry Mumber 212771-30-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,2,7,7 and 1 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 212771-30:
(8*2)+(7*1)+(6*2)+(5*7)+(4*7)+(3*1)+(2*3)+(1*0)=107
107 % 10 = 7
So 212771-30-7 is a valid CAS Registry Number.

212771-30-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[2-[4-(chloromethyl)phenoxy]ethyl]azepane

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:212771-30-7 SDS

212771-30-7Relevant academic research and scientific papers

Benzothieno[3,2-b]indole derivatives as potent selective estrogen receptor modulators

Ji, Qinggang,Gao, Jie,Wang, Junbo,Yang, Chunhao,Hui, Xin,Yan, Xueming,Wu, Xihan,Xie, Yuyuan,Wang, Ming-Wei

, p. 2891 - 2893 (2007/10/03)

A series of estrogen receptor ligands based on benzothieno[3,2-b]indole were synthesized and their binding affinity for estrogen receptor subtypes (ERα and ERβ) and effects on mouse uterus and bone were evaluated. Some of these compounds showed strong bin

N-SUBSTITUTED INDOLINES AS ESTROGENIC AGENTS

-

Page 11, (2008/06/13)

The present invention provides compounds of formula (I) wherein R1 is H or benzyl; R2 is H, -OH, or -O-benzyl; R3, R4, and R5 are independently selected from H, halogen, cyano, C1-C6 alkyl (straight chain or branched), trifluoromethyl, -OH or the C1-C12 e

N-substituted indolines as estrogenic agents

-

, (2008/06/13)

This invention provides compounds of the formula wherein R1, R2, R3, R4, R5, R6, R7, X, n and Y, are as defined in the specification, or a pharmaceutically acceptable salt thereof, as well as pharmaceutical compositions and methods utilizing the compounds for treating or preventing disease states or syndromes which are caused or associated with an estrogen deficiency or an excess of estrogen utilizing these compounds.

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