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Carbonic acid, 2-bromo-3-hydroxy-4-(3-methylbutyl)phenyl 1,1-dimethylethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

680997-59-5

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680997-59-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 680997-59-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,0,9,9 and 7 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 680997-59:
(8*6)+(7*8)+(6*0)+(5*9)+(4*9)+(3*7)+(2*5)+(1*9)=225
225 % 10 = 5
So 680997-59-5 is a valid CAS Registry Number.

680997-59-5SDS

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 [1-[2-bromo-3-hydroxy-4-(3-methylbutyl)phenyl]-2-methylpropan-2-yl] carbonate

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:680997-59-5 SDS

680997-59-5Relevant academic research and scientific papers

Total synthesis of (+)-rishirilide B: Development and application of general processes for enantioselective oxidative dearomatization of resorcinol derivatives

Mejorado, Lupe H.,Pettus, Thomas R. R.

, p. 15625 - 15631 (2007/10/03)

A concise synthesis of (+)-rishirilide B (2) is described. This is the first synthesis to be reported for the (+)-enantiomer of rishirilide B (2) as found in nature. The strategy accentuates the valuable combination of a method for oquinone methide coupli

Diastereoselective dearomatization of resorcinols directed by a lactic acid tether: Unprecedented enantioselective access to p-quinols

Mejorado, Lupe H.,Hoarau, Christophe,Pettus, Thomas R. R.

, p. 1535 - 1538 (2007/10/03)

An operationally simple oxidative dearomatization of resorcinol derivatives is reported that employs an inexpensive chiral directing group. The method provides access to a variety of p-quinol derivatives in good yield and diastereoselectivity. A short red

Cycloadditions of o-quinone dimethides with p-quinol derivatives: Regiocontrolled formation of anthracyclic ring systems

Wang, Junhua,Pettus, Liping H.,Pettus, Thomas R. R.

, p. 1793 - 1796 (2007/10/03)

Regioselective cycloadditions between the cyclohexadienones 12-14 and the ortho-quinone dimethide 19, which is thermally generated from the corresponding 1,3-dihydro-1-methoxy-2,2-dioxide benzo[c]thiophene 27, are reported. The synthetic sequence provides

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