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Benzene, 2-(1-cyclohexen-1-ylmethyl)-1-methoxy-3-(methoxymethoxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

127462-76-4

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127462-76-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 127462-76-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,4,6 and 2 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 127462-76:
(8*1)+(7*2)+(6*7)+(5*4)+(4*6)+(3*2)+(2*7)+(1*6)=134
134 % 10 = 4
So 127462-76-4 is a valid CAS Registry Number.

127462-76-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(1'-CYCLOHEXENYL)-METHYL-3-METHOXYMETHOXYANISOLE

1.2 Other means of identification

Product number -
Other names 2-(1'-cyclohexenylmethyl)-1-methoxy-3-(methoxymethoxy)benzene

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:127462-76-4 SDS

127462-76-4Relevant academic research and scientific papers

Compounds that inhibit complement and/or suppress immune activity

-

, (2008/06/13)

The present invention is directed to compounds which suppress immune responses and/or selectively inhibit complement. These compounds contain an aromatic ring and are substituted dihydrobenzofurans, spirobenzofuran-2(3H)-cycloalkanes, and their open chain intermediates. The compounds of the present invention, and the pharmaceutically acceptable salts thereof, interrupt the proteolytic processing of C5 to bioactive components, exhibit immunosuppressive activities, and have therapeutic utility in the amelioration of disease and disorders mediated by complement and/or immune activity.

Compounds which inhibit complement and/or suppress immune activity

-

, (2008/06/13)

The present invention is directed to compounds which suppress immune responses and/or selectively inhibit complement. These compounds contain an aromatic ring and are substituted dihydrobenzofurans, spirobenzofuran-2(3H)-cycloalkanes, and their open chain intermediates. The compounds of the present invention, and the phamaceutically acceptable salts thereof, interrupt the proteolytic processing of C5 to bioactive components, exhibit immunosuppressive activites, and have therapeutic utility in the amelioration of disease and disorders mediated by complement and/or immune activity.

Compounds which inhibit complement and/or suppress immune activity

-

, (2008/06/13)

The present invention is directed to compounds which suppress immune responses and/or selectively inhibit complement. These compounds contain an aromatic ring and are substituted dihydrobenzofurans, spirobenzofuran-2(3H)-cycloalkanes, and their open chain intermediates. The compounds of the present invention, and the pharmaceutically acceptable salts thereof, interrupt the proteolytic processing of C5 to bioactive components, exhibit immunosuppressive activities, and have therapeutic utility in the amelioration of disease and disorders mediated by complement and/or immune activity.

Synthesis of 4,7-Disubstituted Spirobenzofuran-2(3H)-cyclohexanes

Bradbury, Barton J.,Sindelar, Robert D.

, p. 1827 - 1833 (2007/10/02)

A general synthetic strategy was designed for the preparation of 7-substituted-4-methoxy- and 4-hydroxyspiro 5 and 6 (Figure 1) using successive, regioselective heteroatom-facilitated aromatic lithiation reactions and subsequent reaction with various electrophiles.

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