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N-[bis(4-methoxyphenyl)methyl]formamide is a complex organic compound with the molecular formula C18H19NO4. It is characterized by a formamide group (HCONH) attached to a central carbon atom, which is bonded to two 4-methoxyphenyl groups. The 4-methoxyphenyl groups each contain a phenyl ring with a methoxy substituent at the para position. N-[bis(4-methoxyphenyl)methyl]formamide is known for its potential applications in the synthesis of various pharmaceuticals and chemical intermediates due to its unique structure and reactivity. It is typically synthesized through a series of chemical reactions and is used in research and development for creating new compounds with specific properties.

6063-68-9

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6063-68-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6063-68-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,6 and 3 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6063-68:
(6*6)+(5*0)+(4*6)+(3*3)+(2*6)+(1*8)=89
89 % 10 = 9
So 6063-68-9 is a valid CAS Registry Number.

6063-68-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-butyl-1,3-dimethyl-[1,3,2]diazaborinane

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

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More Details:6063-68-9 SDS

6063-68-9Downstream Products

6063-68-9Relevant 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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