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98799-41-8

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98799-41-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 98799-41-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,7,9 and 9 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 98799-41:
(7*9)+(6*8)+(5*7)+(4*9)+(3*9)+(2*4)+(1*1)=218
218 % 10 = 8
So 98799-41-8 is a valid CAS Registry Number.

98799-41-8SDS

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-iodo-3,4,5-trimethoxybenzoic acid

1.2 Other means of identification

Product number -
Other names 2-Jod-3,4,5-trimethoxy-benzoesaeure

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:98799-41-8 SDS

98799-41-8Relevant articles and documents

Synthesis, characterization, and crystal structure of 2-iodo-3,4,5- trimethoxybenzoic acid

Kolev, Iliyan N.,Petrova, Svetlana P.,Nikolova, Rositsa P.,Dimowa, Louiza T.,Shivachev, Boris L.

, p. 318 - 324 (2013)

This work describes the synthesis of 2-iodo-3,4,5-trimethoxybenzoic acid. The combination of iodine and silver trifluoroacetate (AgTFA) reagents was used successfully for the iodination of 3,4,5-trimetoxybenzoic acid. To improve the efficiency of the synt

Total Synthesis of (+)-Isoschizandrin Utilizing a Samarium(II) Iodide-Promoted 8-Endo Ketyl-Olefin Cyclization

Molander, Gary A.,George, Kelly M.,Monovich, Lauren G.

, p. 9533 - 9540 (2007/10/03)

The 13-step synthesis of (+)-isoschizandrin reported herein features a samarium(II) iodide-promoted 8-endo ketyl-olefin coupling to assemble the eight-membered ring present in the target concomitantly with the required functionality and stereochemistry. In constructing (+)-isoschizandrin as a single atropisomer, the synthesis utilizes a kinetic resolution of a seven-membered lactone using a CBS-oxazaborolidine.

Synthesis of 3,4-O-(3,3',4,4',5,5'-Hexamethoxydiphenoyl)-L-arabinopyranose

Trivedi, K. K.,Kochak, Geeta,Misra, K.

, p. 925 - 926 (2007/10/02)

3,4-O-(3,3',4,4',5,5'-Hexamethoxydiphenoyl)-L-arabinopyranose (Ib) has been synthesized by condensation of 1-O-(3,4,5-tri-O-methylgalloyl)-L-arabinose (IV) with hexamethoxydiphenoyl chloride (IIIb) in pyridine in the presence of triethylamine and subsequent removal of the protecting galloyl group.The synthetic Ib has been found to be identical (m.m.p., co-TLC, IR) with methyl ether of the natural 3,4-O-(3,3',4,4',5,5'-hexahydroxyphenoyl)-L-arabinopyranose (Ia).

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