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35674-27-2

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35674-27-2 Usage

Uses

4-Iodo-3-nitrobenzoic acid is used as a pharmaceutical intermediate.

Check Digit Verification of cas no

The CAS Registry Mumber 35674-27-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,6,7 and 4 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 35674-27:
(7*3)+(6*5)+(5*6)+(4*7)+(3*4)+(2*2)+(1*7)=132
132 % 10 = 2
So 35674-27-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H4INO4/c8-5-2-1-4(7(10)11)3-6(5)9(12)13/h1-3H,(H,10,11)

35674-27-2 Well-known Company Product Price

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  • Alfa Aesar

  • (B25626)  4-Iodo-3-nitrobenzoic acid, 97%   

  • 35674-27-2

  • 5g

  • 2190.0CNY

  • Detail
  • Alfa Aesar

  • (B25626)  4-Iodo-3-nitrobenzoic acid, 97%   

  • 35674-27-2

  • 25g

  • 8879.0CNY

  • Detail

35674-27-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-iodo-3-nitrobenzoic acid

1.2 Other means of identification

Product number -
Other names 4-Iodo-3-Nitrobenzoic Acid

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:35674-27-2 SDS

35674-27-2Relevant articles and documents

The solid phase synthesis of tri-substituted indoles

Collini, Michael D.,Ellingboe, John W.

, p. 7963 - 7966 (1997)

The palladium-catalyzed solid phase synthesis of tri-substituted indoles is described. The synthesis incorporates three independently variable groups and is ideally suited for the preparation of combinatorial libraries.

Thermal decomposition pathways of nitro-functionalized metal-organic frameworks

McDonald, Kyle A.,Ko, Nakeun,Noh, Kyungkyou,Bennion, Jonathan C.,Kim, Jaheon,Matzger, Adam J.

, p. 7808 - 7811 (2017)

The decomposition behavior of high energy metal-organic frameworks (MOFs) with extensive nitration is disclosed. In contrast to the detonation behavior observed in molecular energetic compounds, deflagration transforms cubic MOFs into anisotropic carbon s

Inexpensive NaX (X = I, Br, Cl) as a halogen donor in the practical Ag/Cu-mediated decarboxylative halogenation of aryl carboxylic acids under aerobic conditions

Fu, Zhengjiang,Jiang, Ligao,Zuo, Qianming,Li, Zhaojie,Liu, Yanzhu,Wei, Zhenhong,Cai, Hu

, p. 5416 - 5421 (2018/08/12)

Versatile and practical Ag/Cu-mediated decarboxylative halogenation between readily available aryl carboxylic acids and abundant NaX (X = I, Br, Cl) has been achieved under aerobic conditions in moderate to good yields. The halodecarboxylation is shown to be an effective strategy for S-containing heteroaromatic carboxylic acid and benzoic acids with nitro, chloro and methoxyl substituents at the ortho position. A gram-scale reaction and a three-step procedure to synthesize iniparib have been performed to evaluate the practicality of this protocol. A preliminary mechanistic investigation indicates that Cu plays a vital role and a radical pathway is involved in the transformation.

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