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2-Cyclohexene-1-carboxylic acid, 3-[[2-bromo-3-methoxy-4-(phenylmethoxy)phenyl]methyl]-2-methyl-4-oxo -, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

620167-67-1

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620167-67-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 620167-67-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,0,1,6 and 7 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 620167-67:
(8*6)+(7*2)+(6*0)+(5*1)+(4*6)+(3*7)+(2*6)+(1*7)=131
131 % 10 = 1
So 620167-67-1 is a valid CAS Registry Number.

620167-67-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-benzyloxy-2-bromo-3-methoxy-benzyl)-2-methyl-4-oxo-cyclohex-2-enecarboxylic acid methyl ester

1.2 Other means of identification

Product number -
Other names 3-(4-Benzyloxy-2-bromo-3-methoxy-benzyl)-2-methyl-4-oxo-cyclohex-2-enecarboxylic acid methyl ester

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:620167-67-1 SDS

620167-67-1Relevant academic research and scientific papers

General route to 4a-methylhydrofluorene diterpenoids: Total syntheses of (±)-taiwaniaquinones D and H, (±)-taiwaniaquinol B, (±)-dichroanal B, and (±)-dichroanone

Banerjee, Mainak,Mukhopadhyay, Ranjan,Achari, Basudeb,Banerjee, Asish Kr.

, p. 2787 - 2796 (2007/10/03)

A general and convergent route for the synthesis of the 4a-methylhydrofluorene diterpenoids has been established through a common hexahydrofluorenone intermediate (10) obtained via Pd(0)-catalyzed reductive cyclization of a substituted 2-(2-bromobenzyl) methylene cyclohexane (13). The strategy has been successfully utilized for the synthesis of (±)-taiwaniaquinones D (3) and H (5), (±)-taiwaniaquinol B (1), (±)-dichroanal B (7), and (±)-dichroanone (8).

Intramolecular Heck reaction strategy for the synthesis of functionalised tetrahydroanthracenes: A facile formal total synthesis of the linear abietane diterpene, umbrosone

Sengupta, Sujaya,Mukhopadhyay, Ranjan,Achari, Basudeb,Banerjee, Asish Kr.

, p. 1515 - 1519 (2007/10/03)

Rapid annulation employing an intramolecular Heck reaction yielded the functionalised 1,1,10-trimethyl-6-methoxy-1,2,3,4-tetrahydroanthracene 4a, a key intermediate for the linear diterpenoid quinone umbrosone (1), and the related compounds 4b-d. A simila

First Total Synthesis of the 4a-Methyltetrahydrofluorene Diterpenoids (±)-Dichroanal B and (±)-Dichroanone

Banerjee, Mainak,Mukhopadhyay, Ranjan,Achari, Basudeb,Banerjee, Asish Kr.

, p. 3931 - 3933 (2007/10/03)

(Matrix presented) A simple synthesis of the 4a-methyltetrahydrofluorene diterpenoids (±)-dichroanal B and (±)-dichroanone has been achieved through a common hexahydrofluorenone intermediate obtained via Pd(0)-catalyzed reductive cyclization of a substituted 2-(2-bromobenzyl) methylene cyclohexane.

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