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2-(4-dibromomethyl-phenyl)-5,5-dimethyl-[1,3,2]dioxaborinane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1006598-62-4

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1006598-62-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1006598-62-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,6,5,9 and 8 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1006598-62:
(9*1)+(8*0)+(7*0)+(6*6)+(5*5)+(4*9)+(3*8)+(2*6)+(1*2)=144
144 % 10 = 4
So 1006598-62-4 is a valid CAS Registry Number.

1006598-62-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-(dibromomethyl)phenyl)-5,5-dimethyl-1,3,2-dioxaborinane

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:1006598-62-4 SDS

1006598-62-4Relevant academic research and scientific papers

A versatile method for the hydrolysis of gem-dibromomethylarenes bearing carboxylate or boronate group into aldehydes

Augustine, John Kallikat,Naik, Y. Arthoba,Mandal, Ashis Baran,Chowdappa, Nagaraja,Praveen, Vinuthan B.

, p. 688 - 695 (2008/04/12)

Hydrolysis of gem-dibromomethylarenes bearing carboxylate or boronate group to corresponding aldehydes without affecting the ester group was successfully accomplished in high yields by subjecting them to refluxing pyridine. Both aromatic and heteroaromatic substrates gave the corresponding aldehydes in good yields. This method was efficiently adapted for the large scale synthesis of 2d and 2f.

14C-labeled and large-scale synthesis of the angiotensin-(1-7)-receptor agonist AVE 0991 by cross-coupling reactions.

Derdau, Volker,Oekonomopulos, Raymond,Schubert, Gerrit

, p. 5168 - 5173 (2007/10/03)

The synthesis of (14)C-labeled AVE 0991 ((14)()C-1a) and large-scale synthesis of AVE 0991 (1a) are described. In the key step of the synthesis, the C-C coupling reaction of the imidazole (2) and thiophene (3) building blocks was studied under Suzuki and Stille reaction conditions, respectively. Suzuki reaction gave only moderate yields, whereas the best results were obtained under Stille reaction conditions with up to 64% yield.

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