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1,3-Benzenediol, 2,4-diiodo- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

41046-69-9

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41046-69-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41046-69-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,0,4 and 6 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 41046-69:
(7*4)+(6*1)+(5*0)+(4*4)+(3*6)+(2*6)+(1*9)=89
89 % 10 = 9
So 41046-69-9 is a valid CAS Registry Number.

41046-69-9SDS

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 2,4-diiodobenzene-1,3-diol

1.2 Other means of identification

Product number -
Other names 2,4-Diiod-resorcin

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:41046-69-9 SDS

41046-69-9Upstream product

41046-69-9Relevant academic research and scientific papers

Iodination of anilines and phenols with 18-crown-6 supported ICl 2-

Mbatia, Hannah W.,Ulloa, Olbelina A.,Kennedy, Daniel P.,Incarvito, Christopher D.,Burdette, Shawn C.

experimental part, p. 2987 - 2991 (2011/06/16)

A highly crystalline iodinating reagent, {[K·18-C-6]ICl 2}n, was synthesized in high yield (93%). The trihalide is supported by an 18-crown-6 macrocycle and forms a coordination polymer in the solid state. This reagent iodinates anilines and phenols efficiently under mild conditions. Controlled mono-iodination with anilines was easily achieved while poly-iodination was observed with phenols.

Total synthesis of the antibiotic erypoegin H and cognates by a PtCl 2-catalyzed cycloisomerization reaction

Fuerstner, Alois,Heilmann, Eike K.,Davies, Paul W.

, p. 4760 - 4763 (2008/02/08)

(Chemical Equation Presented) Fighting back: A concise route to the pterocarpene derivative erypoegin H, a natural product endowed with considerable activity against a range of methicillin-resistant Staphyllococcus aureus strains and vancomycin-resistant

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