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5-Cyclopropyl-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-ol is a complex organic compound with the molecular formula C20H21O. It is a derivative of dibenzo[a,d]cyclohepten, a type of tricyclic compound with a cyclopropyl group attached to the 5-position. 5-Cyclopropyl-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-ol is characterized by its unique structure, which includes a cyclohexane ring fused to two benzene rings, with a hydroxyl group at the 5-position. It is a synthetic compound that may have potential applications in pharmaceuticals or as a chemical intermediate due to its specific structural features. However, it is important to note that the compound's specific uses, safety, and environmental impact would need to be thoroughly evaluated, as this information is not provided in the context of the question.

3241-97-2

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3241-97-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3241-97-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,4 and 1 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3241-97:
(6*3)+(5*2)+(4*4)+(3*1)+(2*9)+(1*7)=72
72 % 10 = 2
So 3241-97-2 is a valid CAS Registry Number.

3241-97-2SDS

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 5-cyclopropyl-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-ol

1.2 Other means of identification

Product number -
Other names 5-Cyclopropyl-5-hydroxy-10,11-dihydro-5H-dibenzo[a.d]-cyclohepten

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:3241-97-2 SDS

3241-97-2Relevant academic research and scientific papers

OLIGOMER-TRICYCLIC CONJUGATES

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Paragraph 0298 - 0301, (2016/10/10)

The invention provides small molecule drugs that are chemically modified by covalent attachment of a water soluble oligomer. A conjugate of the invention, when administered by any of a number of administration routes, exhibits characteristics that are different from the characteristics of the small molecule drug not attached to the water soluble oligomer.

Synthesis and SAR study of diphenylbutylpiperidines as cell autophagy inducers

Chen, Gang,Xia, Hongguang,Cai, Yu,Ma, Dawei,Yuan, Junying,Yuan, Chengye

scheme or table, p. 234 - 239 (2011/02/26)

A novel series of diphenylbutylpiperidines as autophagy inducers was described and extensive SAR studies resulted in derivatives (15d-e, 15i-j) with 10-fold greater activity than the lead compounds 1 and 2. Meanwhile, a new synthetic route to diphenylbutyl bromide (6) from bromobenzene and γ-butyrolactone was also reported here.

DIPHENYLBUTYPIPERIDINE AUTOPHAGY INDUCERS

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Page/Page column 7; 84-85, (2011/12/02)

Autophagy inducing compounds, methods of their preparation and use, and kits containg said compounds are disclosed herein.

Method of reducing blood glucose

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, (2008/06/13)

The present invention relates to the use of compounds of the general formula STR1 for reducing blood glucose and/or inhibit the secretion, circulation or effect of insulin antagonizing peptides like CGRP or amylin. Hence the compound can be used in the treatment of insulin resistance related to NIDDM (non-insulin-dependent diabetes mellitus) or aging.

N-substituted azaheterocyclic carboxylic acids and esters thereof

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, (2008/06/13)

The present invention relates to novel N-substituted azaheterocyclic carboxylic acids and esters thereof in which a substituted alkyl chain forms part of the N-substituent or salts thereof, to methods for their preparation, to compositions containing them, and to their use for the clinical treatment of painful, hyperalgesic and/or inflammatory conditions in which C-fibers play a pathophysiological role by eliciting neurogenic pain or inflammation.

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