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81416-99-1

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81416-99-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81416-99-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,4,1 and 6 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 81416-99:
(7*8)+(6*1)+(5*4)+(4*1)+(3*6)+(2*9)+(1*9)=131
131 % 10 = 1
So 81416-99-1 is a valid CAS Registry Number.

81416-99-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-aminoethyl)-4-azidobenzamide

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:81416-99-1 SDS

81416-99-1Downstream Products

81416-99-1Relevant articles and documents

Novel Carbazole (Cbz)-Based Carboxylated Functional Monomers: Design, Synthesis, and Characterization

Mondal, Ejabul,Lellouche, Jean-Paul,Naddaka, Maria

, p. 489 - 496 (2015/10/05)

A series of novel functional carbazole (Cbz)-based carboxylated monomers were synthesized and characterized. A Clauson-Kaas procedure, a deprotection step, amide coupling, and hydrolysis were utilized as key chemical reactions towards the multistep synthesis of monomers in good to excellent isolated yields. The design strategy was further extended to complex carbazole-COOH monomers incorporated arylazo groups as photoreactive moieties. In addition, photoreactive hybrid carbazole (Cbz)-pyrrole (Pyr)-based carboxylated monomers, comprising a pyrrole core linking a carbazole and a photoreactive phenylazide or benzophenone moiety through an amide spacer in the molecular structure, were also synthesized. The latter can be utilized for surface modification of polymeric films in their monomeric form or as polymeric microparticles (MPs). Functional monomers: Novel functional carbazole-based carboxylated monomers were accessed using a Clauson-Kaas procedure, a deprotection step, amide coupling, and hydrolysis in a multistep synthesis. The design strategy was extended to complex carbazole-COOH monomers incorporating arylazo and phenylazide or benzophenone as photoreactive moieties, which can be utilized for functionalization/decoration of various polymeric and non-polymeric surfaces, matrices, and non-functional nanomaterials in their monomeric states or as polymeric microparticles (MPs).

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