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38475-36-4

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38475-36-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38475-36-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,4,7 and 5 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 38475-36:
(7*3)+(6*8)+(5*4)+(4*7)+(3*5)+(2*3)+(1*6)=144
144 % 10 = 4
So 38475-36-4 is a valid CAS Registry Number.

38475-36-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-bromo-5-tert-butyl-1,2-dihydroxybenzene

1.2 Other means of identification

Product number -
Other names 3-bromo-5-tert-butyl-pyrocatechol

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:38475-36-4 SDS

38475-36-4Upstream product

38475-36-4Relevant articles and documents

Electrocatalytic CO2 Reduction to Formate with Molecular Fe(III) Complexes Containing Pendent Proton Relays

Dickie, Diane A.,Hooe, Shelby L.,Kuehner, Joseph S.,Machan, Charles W.,Nichols, Asa W.

, (2020)

Previously, we reported an iron(III) complex with 6,6′-([2,2′-bipyridine]-6,6′-diyl)bis(2,4-ditertbutyl-phenol) as a ligand (Fe(tbudhbpy)Cl, 1) as catalytically competent for the electrochemical reduction of CO2 to formate (Faradaic

Enantioselective organocatalytic aryloxylation of β-keto esters

Greenaway, Kevin,Dambruoso, Paolo,Ferrali, Alessandro,Hazelwood, Andrew J.,Sladojevich, Filippo,Dixon, Darren J.

supporting information; experimental part, p. 1880 - 1886 (2011/07/31)

An efficient enantioselective aryloxylation of cyclic β-keto esters with a selection of substituted o-quinones catalyzed by a bifunctional cinchona alkaloid derivative, giving entry to tricyclic dioxin adducts with high enantio- and diastereoselectivity, is described. Georg Thieme Verlag Stuttgart - New York.

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