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197243-48-4

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197243-48-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 197243-48-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,7,2,4 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 197243-48:
(8*1)+(7*9)+(6*7)+(5*2)+(4*4)+(3*3)+(2*4)+(1*8)=164
164 % 10 = 4
So 197243-48-4 is a valid CAS Registry Number.

197243-48-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Iodo-3-nitrophenol

1.2 Other means of identification

Product number -
Other names 2-Jod-3-nitro-phenol

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:197243-48-4 SDS

197243-48-4Relevant articles and documents

Substituted Fused Heteroaromatic Tricyclic Compounds as Kinase Inhibitors and The Use Thereof

-

Paragraph 0166; 0203, (2021/05/07)

The disclosure relates to substituted fused heteroaromatic tricyclic compounds and the use thereof. Specifically, the disclosure provides compounds of the following Formula I: or a pharmaceutically acceptable salt or prodrug thereof, wherein A1

Synthetic method for optically pure double-helix oligomeric tetra-benzocyclooctene substances

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Paragraph 0033; 0034; 0035, (2017/07/31)

The invention discloses a synthetic method for optically pure double-helix oligomeric tetra-benzocyclooctene substances. The synthetic method comprises the following steps: (1) carrying out oxidative cross-coupling on diiodo dimethoxy biphenyl (51) and 2,2',6,6'-biphenyl tetrabromide (97) to obtain 1,16-dibromo-8,9-dimethoxy tetra-benzocyclooctene (96); (2) splitting the compound (96), thus obtaining optically pure (S, S)-96 and (R, R)-96; (3) taking the compound (96) as a raw material, synthesizing an intermediate (116) containing 6 benzene rings; (4) splitting the intermediate (116) to obtain (M)-116 and (P)-116; (5) making the optically pure (S, S)-96 and (M)-116 reacted to obtain target products, namely (M) -117, (M)-149 and (M)-150; and/or: making the (R, R)-96 and (P)-116 reacted to obtain target products, namely (P)-117, (P)-149 and (P)-150.

Total synthesis of dictyodendrins B and E, and formal synthesis of dictyodendrin C

Tao, Pengyu,Liang, Jingjing,Jia, Yanxing

, p. 5735 - 5748 (2014/11/07)

A full account of the concise total syntheses of dictyodendrins B and E, and the formal synthesis of dictyodendrin C are described. A palladium-catalysed Larock indole synthesis was used to form the highly substituted indole core, and a palladium-mediated

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