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354512-22-4

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354512-22-4 Usage

General Description

3-Methoxy-5-nitrobenzaldehyde is a chemical compound with the molecular formula C8H7NO4. It is a yellow solid with a strong odor, and it is commonly used in the pharmaceutical and dye industries. 3-METHOXY-5-NITROBENZALDEHYDE is often employed as an intermediate in the synthesis of various pharmaceuticals and organic compounds. It is also used as a reagent in organic synthesis and as a starting material for the preparation of other benzaldehyde derivatives. Additionally, 3-methoxy-5-nitrobenzaldehyde is known for its antibacterial and antifungal properties, and it has potential applications in the development of new drugs and biologically active compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 354512-22-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,4,5,1 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 354512-22:
(8*3)+(7*5)+(6*4)+(5*5)+(4*1)+(3*2)+(2*2)+(1*2)=124
124 % 10 = 4
So 354512-22-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H7NO4/c1-13-8-3-6(5-10)2-7(4-8)9(11)12/h2-5H,1H3

354512-22-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-METHOXY-5-NITROBENZALDEHYDE

1.2 Other means of identification

Product number -
Other names Benzaldehyde,3-methoxy-5-nitro

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:354512-22-4 SDS

354512-22-4Downstream Products

354512-22-4Relevant articles and documents

Structure-activity relationship of 7-aryl-2-anilino-pyrrolopyrimidines as Mer and Axl tyrosine kinase inhibitors

Chung, Shin Hyuck,Park, Jiwon,Lee, Jung Wuk,Song, Jiho,Jung, Danbee,Min, Kyung Hoon

, p. 1822 - 1833 (2020/10/02)

The TAM (Axl, Mer, and Tyro3) family is implicated in the survival and chemoresistance of tumours and has emerged as a potential therapeutic target. A novel series of 7-aryl-2-anilino-pyrrolopyrimidines were identified as potent Axl/Mer tyrosine kinase in

PHENYL-UREA AND PHENYL-CARBAMATE DERIVATIVES AS INHIBITORS OF PROTEIN AGGREGATION

-

, (2013/10/21)

The present invention relates to certain phenyl-urea and phenyl-carbamate derivatives, pharmaceutical compositions containing them, and methods of using them, including methods for preventing, reversing, slowing, or inhibiting protein aggregation, and methods of treating diseases that are associated with protein aggregation, including neurodegenerative diseases such as Parkinson's disease, Alzheimer's disease, Lewy body disease, and multiple system atrophy.

Synthesis and structure-activity relationships of 3-aminobenzophenones as antimitotic agents

Liou, Jing-Ping,Chang, Jang-Yang,Chang, Chun-Wei,Chang, Chi-Yen,Mahindroo, Neeraj,Kuo, Fu-Ming,Hsieh, Hsing-Pang

, p. 2897 - 2905 (2007/10/03)

A new series of 3-aminobenzophenone compounds as potent inhibitors of tubulin polymerization was discovered based on the mimic of the aminocombretastatin molecular skeleton. Lead compounds 5 and 11, with alkoxy groups at the C-4 position of B-ring, were p

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