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82185-43-1

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82185-43-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82185-43-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,1,8 and 5 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 82185-43:
(7*8)+(6*2)+(5*1)+(4*8)+(3*5)+(2*4)+(1*3)=131
131 % 10 = 1
So 82185-43-1 is a valid CAS Registry Number.

82185-43-1SDS

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 2-methyl-N-trimethylsilylaniline

1.2 Other means of identification

Product number -
Other names Silanamine,1,1,1-trimethyl-N-(2-methylphenyl)

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:82185-43-1 SDS

82185-43-1Relevant articles and documents

Indole diterpenoid synthetic studies. The total synthesis of (+)-nodulisporic acid F

Smith III, Amos B.,Davulcu, Akin H.,Kuerti, Laszlo

, p. 1665 - 1668 (2006)

A stereocontrolled total synthesis of (+)-nodulisporic acid F, the simplest member of a family of novel ectoparasiticidal agents, has been achieved. Highlights of the effective modular synthetic strategy include anionic union of a tricyclic lactone with o

A highly facile approach to the synthesis of novel 2-(3-benzyl-2,4-dioxo-1, 2,3,4-tetrahydropyrimidin-1-yl)-N-phenylacetamides

Novikov, Mikhail S.,Babkov, Denis A.,Paramonova, Maria P.,Chizhov, Alexander O.,Khandazhinskaya, Anastasia L.,Seley-Radtke, Katherine L.

supporting information, p. 576 - 578 (2013/02/23)

A series of heterocyclic compounds were designed as potential nonnucleoside HIV reverse transcriptase inhibitors. Although the compounds ultimately proved inactive against HIV, during the course of the synthesis, a new and highly facile method to realize N-phenylacetamides was developed. Notably, the new route avoids the intractable workups and byproducts previously reported procedures have been associated with, thereby making this approach highly attractive to adaptation with other heterocyclics.

13C, 15N and 29Si nuclear magnetic resonance studies of some aminosilanes and aminodisilanes

Wrackmeyer, Bernd,Stader, Carin,Zhou, Hong

, p. 1101 - 1112 (2007/10/02)

13C, 15N (at natural abundance) and 29Si NMR data (chemical shifts and coupling constants) are reported for aminosilanes R2R'Si-NHR1 (1), bis(silyl)amines Me2R'Si-NHSiMe3 (2), 1,2-bis(amino)ethanes (3), bis(amin

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