313735-67-0

Basic information

• Product Name: 1-ISOPROPYL-1H-PYRAZOLE-4-CARBALDEHYDE
• Synonyms: CHEMBRDG-BB 4003133;1-ISOPROPYL-1H-PYRAZOLE-4-CARBALDEHYDE;AKOS PAO-0278;1H-Pyrazole-4-carboxaldehyde, 1-(1-methylethyl)- (9CI);1-Isopropyl-1H-pyrazole-4-carboxaldehyde;1-isopropyl-1H-pyrazole-4-carbaldehyde(SALTDATA: FREE);1-isopropyl-4-pyrazolecarboxaldehyde;1-isopropylpyrazole-4-carbaldehyde
• CAS NO: 313735-67-0
• Molecular Formula: C7H10N2O
• Molecular Weight: 138.17
• Product Categories: ALDEHYDE
• Mol File: 313735-67-0.mol

Chemical Properties

• Boiling Point: 228.9°C at 760 mmHg
• Flash Point: 92.2°C
• Appearance: /
• Density: 1.08g/cm³
• Vapor Pressure: 0.0717mmHg at 25°C
• Refractive Index: 1.535
• Storage Temp.: Room temperature.
• PKA: 0.21±0.10(Predicted)
• CAS DataBase Reference: 1-ISOPROPYL-1H-PYRAZOLE-4-CARBALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-ISOPROPYL-1H-PYRAZOLE-4-CARBALDEHYDE(313735-67-0)
• EPA Substance Registry System: 1-ISOPROPYL-1H-PYRAZOLE-4-CARBALDEHYDE(313735-67-0)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 313735-67-0(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
1-Isopropyl-1H-pyrazole-4-carbaldehyde is used as a chemical intermediate for the synthesis of more complex molecules. Its unique structure allows for the creation of a variety of pharmaceutical compounds, contributing to the development of new drugs and therapeutic agents.
Used in Research and Development:
In the field of chemical research, 1-Isopropyl-1H-pyrazole-4-carbaldehyde is employed as a starting material for the exploration of new chemical reactions and the synthesis of novel compounds. Its reactivity and structural features make it a valuable tool for advancing scientific understanding and discovering new applications in various industries.
Used in Material Science:
The properties of 1-Isopropyl-1H-pyrazole-4-carbaldehyde may also be harnessed in material science applications, where its chemical structure could be utilized to develop new materials with specific characteristics. This could include the creation of advanced materials for use in electronics, coatings, or other specialized applications.

InChI:InChI=1/C7H10N2O/c1-6(2)9-4-7(5-10)3-8-9/h3-6H,1-2H3

Upstream product

• 75-30-9 2-iodo-propane 
• 35344-95-7 1H-pyrazole-4-carbaldehyde 
• 68-12-2 N,N-dimethyl-formamide 
• 18952-87-9 1-isopropyl-1H-pyrazole 
• 313735-62-5 4-bromo-1-(propan-2-yl)-1H-pyrazole 

Downstream Products

• 958948-25-9 C₂₂H₃₁N₃O₂ 

Relevant articles and documents

CEREBLON BINDERS FOR THE DEGRADATION OF IKAROS

The present invention provides cereblon binders for the degradation of Ikaros or Aiolos by the ubiquitin proteasome pathway along with their use in therapeutic applications as described herein.

THERAPEUTIC COMPOUNDS AND USES THEREOF

The present invention relates to compounds useful as inhibitors of one or more histone demethylses, such as KDM5. The invention also provides pharmaceutically acceptable compositions comprising compounds of the present invention and methods of using said

Synthesis of heterocyclic compounds from 4-formylpyrazoles

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

BENZAZEPINE DERIVATIVES, PROCESS FOR THE PREPARATION OF THE SAME AND USES THEREOF

Compounds of the general formula (I): or salts thereof, which exhibit CCR5 antagonism and exert preventive and therapeutic effects against HIV infections: wherein R1 is a 5- to 6-membered aromatic ring which bears a substituent represented by the general formula: R-Z1-X-Z2- (wherein R1 is hydrogen or optionally substituted hydrocarbyl; X is optionally substituted alkylene; and Z1 and Z2 are each a heteroatom) and may be further substituted, with R being optionally bonded to the aromatic ring to form another ring; Y is optionally substituted imino; and R2 and R3 are each optionally substituted aliphatic hydrocarbyl or an optionally substituted hetero-alicyclic group.