Welcome to LookChem.com Sign In|Join Free

CAS

  • or

890626-07-0

1-ISOPROPYL-3,5-DIMETHYL-1H-PYRAZOLE-4-CARBALDEHYDE is a chemical compound with the molecular formula C10H16N2O. It is a derivative of pyrazole and belongs to the class of aldehydes. 1-ISOPROPYL-3,5-DIMETHYL-1H-PYRAZOLE-4-CARBALDEHYDE is characterized by its sweet, floral, and fruity odor, making it a valuable ingredient in the fragrance and flavor industry.
Used in Fragrance and Flavor Industry:
1-ISOPROPYL-3,5-DIMETHYL-1H-PYRAZOLE-4-CARBALDEHYDE is used as a fragrance and flavoring agent for its ability to enhance the overall scent and taste of various products such as perfumes, cosmetics, and food.
Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, 1-ISOPROPYL-3,5-DIMETHYL-1H-PYRAZOLE-4-CARBALDEHYDE may have potential applications in the pharmaceutical industry, possibly due to its chemical properties and structure.
Used in Agrochemical Industry:
Similarly, the compound may also have potential uses in the agrochemical industry, although specific applications are not detailed in the provided materials. Its potential use could be related to its ability to influence the scent or taste of agricultural products or as a component in developing new agrochemical products.
It is important to handle 1-ISOPROPYL-3,5-DIMETHYL-1H-PYRAZOLE-4-CARBALDEHYDE with care and follow proper safety precautions due to its potential hazards.

890626-07-0 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 890626-07-0 Structure

  • Basic information

    1. Product Name: 1-ISOPROPYL-3,5-DIMETHYL-1H-PYRAZOLE-4-CARBALDEHYDE
    2. Synonyms: AKOS BBS-00005797;AKOS PAO-0281;1-ISOPROPYL-3,5-DIMETHYL-1H-PYRAZOLE-4-CARBALDEHYDE;ASINEX-REAG BAS 03439166;1-isopropyl-3,5-dimethyl-4-pyrazolecarboxaldehyde;1-isopropyl-3,5-dimethyl-pyrazole-4-carbaldehyde;3,5-dimethyl-1-propan-2-yl-pyrazole-4-carbaldehyde;3,5-dimethyl-1-propan-2-ylpyrazole-4-carbaldehyde
    3. CAS NO:890626-07-0
    4. Molecular Formula: C9H14N2O
    5. Molecular Weight: 166.22
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 890626-07-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-ISOPROPYL-3,5-DIMETHYL-1H-PYRAZOLE-4-CARBALDEHYDE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-ISOPROPYL-3,5-DIMETHYL-1H-PYRAZOLE-4-CARBALDEHYDE(890626-07-0)
    11. EPA Substance Registry System: 1-ISOPROPYL-3,5-DIMETHYL-1H-PYRAZOLE-4-CARBALDEHYDE(890626-07-0)

  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 890626-07-0(Hazardous Substances Data)

890626-07-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 890626-07-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,0,6,2 and 6 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 890626-07:
(8*8)+(7*9)+(6*0)+(5*6)+(4*2)+(3*6)+(2*0)+(1*7)=190
190 % 10 = 0
So 890626-07-0 is a valid CAS Registry Number.

890626-07-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-dimethyl-1-propan-2-ylpyrazole-4-carbaldehyde

1.2 Other means of identification

Product number -
Other names BB_SC-9096

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:890626-07-0 SDS

890626-07-0Downstream Products

890626-07-0Relevant articles and documents

FUSED IMIDAZOPYRIDINES AS REVERSIBLE INHIBITORS OF BRUTON'S TYROSINE KINASE (BTK)

-

Paragraph 00174, (2020/03/23)

The present invention relates to fused imidazo pyridine compounds of formula (I), and pharmaceutically acceptable compositions thereof, useful as BTK inhibitors.

2-(pyrazol-4-yl)-1,3-oxaselenolanes from pyrazole carbaldehydes and 2-selanyl-1-ethanol

Papernaya, Lyubov K.,Shatrova, Alexandra A.,Levanova, Ekaterina P.,Albanov, Alexandr I.,Klyba, Lyudmila V.,Rudyakova, Elena V.,Levkovskaya, Galina G.

, p. 5 - 11 (2015/03/03)

Pyrazole carbaldehydes react with 2-selanyl-1-ethanol at room temperature in the presence of trimethylchlorosilane followed by treatment C with triethyl amine to afford the corresponding 2-(pyrazol-4-yl)-1,3-oxaselenolanes. The structure of the novel compounds was confirmed by IR, 13 C, 1 H, 15N, and 77 Se NMR spectroscopy.this article online at wileyonlinelibrary.com.

Synthesis of heterocyclic compounds from 4-formylpyrazoles

Mortikov,Rodinovskaya,Fedorov,Shestopalov,Belyakov

, p. 443 - 456 (2015/02/02)

Formylation of pyrazole and 2,5-dimethylpyrazole gave a number of pyrazole-containing aldehydes, which can be used to obtain chromenes, tetrahydrochromenes, 1,4-dihydropyrano[2,3-c]pyrazoles, pyrano[3,2-c]chromenes, thiochromeno[4,3-b]pyrans, pyrano[3,2-c

Selenoacetalyzation of 4-formylpyrazoles in the presence of trimethylchlorosilane

Papernaya, Lyubov K.,Shatrova, Alexandra A.,Levanova, Ekaterina P.,Albanov, Alexandr I.,Klyba, Lyudmila V.,Rudyakova, Elena V.,Levkovskaya, Galina G.

, p. 466 - 475 (2013/12/04)

The reaction of 3,5-dimethyl-4-formylpyrazoles, bearing various substituents at N-1 atom, with propane-1,3-diselenol and 2-hydroxypropane-1,3- diselenol in the presence of Cyrillic capital letter teCyrillic capital letter emSCl proceeds without heating to

Fragmentation of pyrazolecarbaldehyde thio- and dithioacetals under electron impact and chemical ionization

Klyba,Papernaya,Sanzheeva,Shatrova,Rudyakova,Levkovskaya

body text, p. 1851 - 1858 (2012/03/11)

The mass spectra of 1-substituted 3,5-dimethyl-1H-pyrazole-4-carbaldehyde bis(2-hydroxyethyl) dithioacetals and thioacetals were studied for the first time. The main fragmentation pathways of their molecular ions generated under electron impact and chemic

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

What can I do for you?
Get Best Price

Get Best Price for 890626-07-0