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N-(2-chloroethyl)-N-(2-nitrobenzyl)acetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1086007-35-3

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1086007-35-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1086007-35-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,8,6,0,0 and 7 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1086007-35:
(9*1)+(8*0)+(7*8)+(6*6)+(5*0)+(4*0)+(3*7)+(2*3)+(1*5)=133
133 % 10 = 3
So 1086007-35-3 is a valid CAS Registry Number.

1086007-35-3Relevant academic research and scientific papers

Simple synthesis process of anxiolytic drug lorazepam intermediate

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Paragraph 0007; 0008; 0019; 0020; 0022 0007; 0008, (2019/05/08)

The invention discloses a simple synthesis process of an anxiolytic drug lorazepam intermediate. The simple synthesis process comprises the steps of putting N-(2-chloroethyl)acetamide, triethylamine and dichloromethane into a reaction bottle; stirring the

Process for Preparing 4-Acetyl-2,3,4,5-tetrahydro-benzo[1,4]diazepine and the Intermediates Thereof

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Page/Page column 5, (2010/10/19)

The present invention relates to a process for preparing 4-acetyl-2,3,4,5-tetrahydro-benzo[1,4]diazepine and the intermediates thereof. The present invention provides a compound represented by formula I and a compound represented by formula II, and proces

PREPARATION METHODS OF 4-ACETYL-2,3,4,5-TETRAHYDRO- BENZO[1,4]DIAZEPINE AND THEIR INTERMEDIATES

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Page/Page column 8, (2010/04/24)

The present invention relates to a process for preparing 4-acetyl-2,3,4,5-tetrahydrobenzo[1,4]diazepine and the intermediates thereof. The present invention provides a compound represented by formula I and a compound represented by formula II, and processes for preparing 4-acetyl-2,3,4,5-tetrahydro-benzo[1,4]diazepine by using the compound represented by formula I, the compound represented by formula II and o-nitrobenzaldehyde. The invention has the advantages of the shorter synthesis steps, easily available raw materials and simple operation. Moreover, the process is economic and safe by avoiding the use of expensive and dangerous lithium aluminium hydride.

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