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30362-89-1

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30362-89-1 Usage

Physical state

White to pale yellow solid

Solubility

Insoluble in water, soluble in organic solvents

Uses

a. Precursor in organic synthesis
b. Production of pharmaceuticals and agrochemicals
c. Building block in the synthesis of polymers and industrial chemicals

Chemical classification

Halogenated aromatic compound

Safety and handling

Use and production should be conducted with relevant safety and handling precautions.

Check Digit Verification of cas no

The CAS Registry Mumber 30362-89-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,3,6 and 2 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 30362-89:
(7*3)+(6*0)+(5*3)+(4*6)+(3*2)+(2*8)+(1*9)=91
91 % 10 = 1
So 30362-89-1 is a valid CAS Registry Number.

30362-89-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-bis(iodomethyl)benzene

1.2 Other means of identification

Product number -
Other names 1,4-di(iodomethyl)benzene

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:30362-89-1 SDS

30362-89-1Relevant articles and documents

Synthesis of novel cyclodextrin derivatives by aromatic spacer insertion and their inclusion ability

Kida, Toshiyuki,Kikuzawa, Akira,Higashimoto, Hiroyuki,Nakatsuji, Yohji,Akashi, Mitsuru

, p. 5763 - 5768 (2005)

Novel cyclic host molecules were synthesized by the insertion of three types of aromatic spacers into the skeleton of permethylated α-cyclodextrin. These host molecules formed a 1:1 complex with sodium 3- and 4-nitrobenzenesulfonates (3- and 4-NBS), and s

Synthesis of new organosilicon compounds by CS2: Mercapto-silyl-thiones

Safa, Kazem D.,Ghorbanpour, Khatereh

, p. 214 - 218 (2013/10/01)

A new type of chemistry of carbon disulfide proceeding by way of nucleophilic attack of tris(trimethylsilyl)methyllithium (TsiLi) at carbon of carbon disulfide is reported. The treatment of TsiLi and CS2 with some symmetrical and unsymmetrical

Silicaphosphine (Silphos): A filterable reagent for the conversion of alcohols and thiols to alkyl bromides and iodides

Iranpoor, Nasser,Firouzabadi, Habib,Jamalian, Arezu,Kazemi, Foad

, p. 5699 - 5704 (2007/10/03)

Silicaphosphine (Silphos), [P(Cl)3-n(SiO2) n], as a new heterogeneous reagent is introduced. This reagent converts alcohols and thiols to their corresponding bromides and iodides in the presence of X2 (X=Br, I) in refluxing CH3CN in high to quantitative yields. Use of Silphos provides a highly practical method for the easy separation of the Silphos oxide byproduct by a simple filtration.

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