Welcome to LookChem.com Sign In|Join Free
  • or
1,2,5-Oxadiazole-3-carboxaldehyde, 4-methyl(9CI) is a chemical compound belonging to the oxadiazole class, characterized by its high reactivity and diverse biological activities, making it a valuable building block in organic synthesis and medicinal chemistry.
Used in Pharmaceutical Industry:
1,2,5-Oxadiazole-3-carboxaldehyde, 4-methyl(9CI) is used as a building block for the synthesis of various biologically active compounds, contributing to the development of new pharmaceuticals.
Used in Agrochemical Industry:
1,2,5-Oxadiazole-3-carboxaldehyde, 4-methyl(9CI) is used as an intermediate in the production of agrochemicals, potentially enhancing the effectiveness of these products.
Used in Organic Dye Industry:
1,2,5-Oxadiazole-3-carboxaldehyde, 4-methyl(9CI) is used as an intermediate for the synthesis of organic dyes, contributing to the creation of new dye formulations.
Used in Drug Discovery:
1,2,5-Oxadiazole-3-carboxaldehyde, 4-methyl(9CI) is used as a promising lead compound in drug discovery due to its diverse biological activities, such as antibacterial, antifungal, and anticancer properties. Further research is needed to fully understand its pharmacological potential and toxicological profile for potential therapeutic applications.

90507-35-0

Post Buying Request

90507-35-0 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

90507-35-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90507-35-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,5,0 and 7 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 90507-35:
(7*9)+(6*0)+(5*5)+(4*0)+(3*7)+(2*3)+(1*5)=120
120 % 10 = 0
So 90507-35-0 is a valid CAS Registry Number.

90507-35-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Methyl-1,2,5-oxadiazole-3-carbaldehyde

1.2 Other means of identification

Product number -
Other names 3-formyl-4-methyl-1,2,5-oxadiazole

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:90507-35-0 SDS

90507-35-0Downstream Products

90507-35-0Relevant academic research and scientific papers

4-[(4-(CARBOXYETHYL) PIPERIDINYL) METHYL] PYRROLIDINES AS MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY

-

Page 33, (2010/02/07)

3-Substituted pyrrolidines having a 4-carboxypiperidinylmethyl substituent on the 4-position of the ring are useful as modulators of chemokine receptor activity. In particular, these compounds are useful as modulators of the chemokine receptors CCR-3 and/or CCR-5.

4(SPIROPIPERIDINYL)METHYL SUBSTITUTED PYRROLIDINES AS MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY

-

Page 42-43, (2010/02/07)

3-Substituted pyrrolidines having a spiropiperidinylmethyl substituent on the 4-position of the ring are useful as modulators of chemokine receptor activity. In particular, these compounds are useful as modulators of the chemokine receptors CCR-3 and/or CCR-5.

Synthesis and cardiovascular properties of furazanyl-1,4-dihydropyridines and of furoxanyl analogues

Gasco,Fruttero,Sorba,Gasco,Budriesi,Chiarini

, p. 921 - 925 (2007/10/02)

A series of furazanyl- and furoxanyl-1,4-dihydropyridines has been synthesized and tested for their cardiovascular activity. The new compounds showed a modest activity in comparison with nifedipine and some selectivity for the myocardial muscle. The most active compound was diethyl 1,4-dihydro-2,6-dimethyl-4-(3-phenyl-4-furoxanyl)3,5-pyridine dicarboxylate, 4d.

Nonquaternary cholinesterase reactivators. II. α-Heteroaromatic aldoximes and thiohydroximates as reactivators of ethyl methylphosphonyl-acetylcholinesterase in vitro

Kenley,Bedford,Dailey Jr.,Howd,Miller

, p. 1201 - 1211 (2007/10/02)

We prepared six pairs of α-heteroaromatic aldoximes, RC(=NOH)H, and thiohydroximates, RC(=NOH)S(CH2)2N(C2H5)2, where R represents various oxadiazole and thiadiazole rings. Each compound was characteri

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 90507-35-0