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36044-41-4

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36044-41-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36044-41-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,0,4 and 4 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 36044-41:
(7*3)+(6*6)+(5*0)+(4*4)+(3*4)+(2*4)+(1*1)=94
94 % 10 = 4
So 36044-41-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H7I/c11-10-6-8-4-2-1-3-5-9(8)7-10/h1-7H

36044-41-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Iodoazulene

1.2 Other means of identification

Product number -
Other names 2-Iodazulen

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:36044-41-4 SDS

36044-41-4Relevant articles and documents

Synthesis and crystal structures of N,N-diarylacetamides bearing two azulene rings

Ito, Ai,Watanabe, Mayuko,Ishii, Ayako,Yamasaki, Ryu,Okamoto, Iwao

supporting information, (2021/11/22)

N,N-Diarylacetamides bearing two azulene rings on the amide nitrogen were synthesized and their crystal structures were determined. The dihedral angle between the amide plane and the aryl ring located on the same side as the amide oxygen atom is influenced by the position of linkage of the aromatic ring to the nitrogen atom, and a 2-azulenyl group located on the same side as amide oxygen atom tends to be coplanar with the amide plane. This feature may be useful in the design of molecular devices and supramolecules.

Synthesis of 2-Iodoazulenes by the Iododeboronation of Azulen-2-ylboronic Acid Pinacol Esters with Copper(I) Iodide

Narita, Masahiro,Murafuji, Toshihiro,Yamashita, Saki,Fujinaga, Masayuki,Hiyama, Kumiko,Oka, Yurie,Tani, Fumito,Kamijo, Shin,Ishiguro, Katsuya

, p. 1298 - 1303 (2018/02/09)

Azulen-2-ylboronic acid pinacol ester, prepared by iridium-catalyzed C-H borylation of azulene, efficiently underwent iododeboronation with a stoichiometric amount of copper(I) iodide. This reaction allowed the synthesis of 2-iodoazulene in only two steps starting from azulene. This methodology was successfully applied to analogous azulenes.

Synthesis and two-electron redox behavior of diazuleno [2,1-a:1,2-c] naphthalenes

Ito, Shunji,Nomura, Akiko,Morita, Noboru,Kabuto, Chizuko,Kobayashi, Hirokazu,Maejima, Seiko,Fujimori, Kunihide,Yasunami, Masafumi

, p. 7295 - 7302 (2007/10/03)

The Diels-Alder reaction of di-2-azulenylacetylene with tetraphenylcyclopentadienone afforded 7,8,9,10-tetraphenyldiazuleno[2,1-a:1,2-c]naphthalene in one pot via autoxidation of the presumed 1,2-di-2-azulenylbenzene derivative. In contrast, a similar rea

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