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1,3,2-Diazaborolidine, 1-ethyl-2-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

5898-35-1

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5898-35-1 Usage

Type of compound

Boron-containing compound

Usage

Chiral catalyst in organic synthesis

Known for

High enantioselectivity in catalysis

Applications

Pharmaceutical and agrochemical industries, materials science

Importance

Versatile and valuable tool in asymmetric synthesis

Structure

Unique structure and reactivity

Check Digit Verification of cas no

The CAS Registry Mumber 5898-35-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,9 and 8 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5898-35:
(6*5)+(5*8)+(4*9)+(3*8)+(2*3)+(1*5)=141
141 % 10 = 1
So 5898-35-1 is a valid CAS Registry Number.

5898-35-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-ethyl-2-phenyl-1,3,2-diazaborolidine

1.2 Other means of identification

Product number -
Other names 1-ethyl-2-phenyl-[1,3,2]diazaborolidine

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:5898-35-1 SDS

5898-35-1Downstream Products

5898-35-1Relevant academic research and scientific papers

Boron-nitrogen compounds. XXV. Substituted 1,3,2-diazaboracycloalkanes

Weber, Wolfgang,Dawson, John W.,Niedenzu, Kurt

, p. 726 - 728 (2008/10/08)

Boron- and nitrogen-substituted 1,3,2-diazaboracycloalkanes have been prepared by a transamination between bis(dimethylamino)boranes and α,ω-diamines. Partial substitution of the nitrogen of the diamine does not appear to inhibit this reaction; five-, six-, and seven-membered heterocyclic systems are readily obtained by the described procedure. However, the low yields of product obtained in those reactions involving an olefinic α,ω-diamine indicate that steric factors may play an important role. The mechanism of the formation of the boron-nitrogen-carbon heterocycles is discussed, and some spectroscopic data are briefly evaluated.

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