Welcome to LookChem.com Sign In|Join Free
  • or
5-Isobenzofurancarboxaldehyde, 1,3-dihydro(9CI), also known as 1,3-dihydro-5-isobenzofurancarboxaldehyde, is a chemical compound with the molecular formula C9H8O2 and a molecular weight of 148.16 g/mol. It is an aldehyde that appears as a pale yellow liquid with a sweet, floral odor.

89424-83-9

Post Buying Request

89424-83-9 Suppliers

Recommended suppliers

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

89424-83-9 Usage

Uses

Used in Food Industry:
5-Isobenzofurancarboxaldehyde, 1,3-dihydro(9CI) is used as a flavoring agent for its sweet, floral scent, enhancing the taste and aroma of various food products.
Used in Perfume and Fragrance Industry:
This chemical compound is also utilized in the production of perfumes and fragrances due to its pleasant and distinctive odor, contributing to the creation of unique and appealing scents.
Used in Pharmaceutical Research:
5-Isobenzofurancarboxaldehyde, 1,3-dihydro(9CI) has been investigated for its potential biological and pharmacological activities. While more research is needed to fully understand its effects on the human body, it holds promise for future medicinal applications.

Check Digit Verification of cas no

The CAS Registry Mumber 89424-83-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,4,2 and 4 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 89424-83:
(7*8)+(6*9)+(5*4)+(4*2)+(3*4)+(2*8)+(1*3)=169
169 % 10 = 9
So 89424-83-9 is a valid CAS Registry Number.

89424-83-9SDS

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 1,3-dihydroisobenzofuran-5-carbaldehyde

1.2 Other means of identification

Product number -
Other names -

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:89424-83-9 SDS

89424-83-9Relevant academic research and scientific papers

PYRAZOLE COMPOUNDS AND METHODS OF MAKING AND USING SAME

-

, (2017/06/12)

Provided herein are pyrazole compounds and pharmaceutical compositions comprising said compounds. The subject compounds and compositions are useful as modulators of MAGL and/or ABHD6. Furthermore, the subject compounds and compositions are useful for the treatment of, for example, pain.

SPIROCYCLE COMPOUNDS AND METHODS OF MAKING AND USING SAME

-

, (2017/12/01)

Provided herein are spirocycle compounds and pharmaceutical compositions comprising said compounds. The subject compounds and compositions are useful as modulators of MAGL and/or ABHD6. Furthermore, the subject compounds and compositions are useful for the treatment of pain.

PESTICIDAL CONDENSED - RING ARYL COMPOUNDS

-

Page/Page column 120-121, (2009/10/22)

Condensed-ring aryl compounds of formula (I) and use of the same as a agrochemical for controlling noxious organisms wherein (X)mQ, A, R1, (Y)n and the grouping -W1-W2-W3-W4- are as defined herein.

AZOLIDINONE-VINYL FUSED-BENZENE DERIVATIVES

-

Page 55, (2008/06/13)

The present invention is related to azolidinedione-vinyl fused-benzene derivatives of formula (I) for the treatment and/or prophylaxis of autoimmune disorders and/or inflammatory diseases, cardiovascular diseases, neurodegenerative diseases, bacterial or viral infections, kidney diseases, platelet aggregation, cancer, graft rejection or lung injuries. Formula (I), wherein A, X, Y, Z, R1 , R2 and n are as described in the description.

Samarium triiodide catalyzed deprotection of 1,1-diacetates

Wang, Xiaoxia,Zhang, Yongmin

, p. 2632 - 2634 (2007/10/03)

Catalyzed by samarium triiodide, cleavage of the 1,1-diacetates proceeds efficiently and selectively to give the corresponding aldehydes under neutral conditions.

1,3-Dioxan-5-ylalkenoic acids

-

, (2008/06/13)

The invention concerns novel 4-phenyl-1,3-dioxan-5-ylalkenoic acid derivatives of the formula I having cis relative stereochemistry at positions 4 and 5 of the dioxane ring and wherein Ra and Rb are variously hydrogen, alkyl, halogenoalkyl, alkenyl, and optionally substituted aryl or arylalkyl, Rc is hydroxy, alkoxy or alkanesulphonamido, n is 1 or 2, A is ethylene or vinylene, Y is (2-5C)polymethylene optionally substituted by alkyl, and benzene ring B is optionally substituted phenyl, or, when Rc is hydroxy, a salt thereof. The acid derivatives antagonize one or more of the actions of thromboxane A2 (TXA2) and are expected to be of value in those disease conditions in which TXA2 is involved. The invention also provides pharmaceutical compositions containing an acid derivative of formula I, and processes for their chemical production.

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 89424-83-9