Welcome to LookChem.com Sign In|Join Free

CAS

  • or

24623-61-8

Post Buying Request

24623-61-8 Suppliers

Recommended suppliersmore

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

24623-61-8 Usage

General Description

2-hydroxy-3,5-dimethylbenzaldehyde is an organic compound with the molecular formula C7H8O2. It is a derivative of benzaldehyde, containing two methyl groups and a hydroxyl group on the aromatic ring. 2-hydroxy-3,5-dimethylbenzaldehyde is commonly used as a building block in the synthesis of various pharmaceuticals, fragrances, and agricultural chemicals. It also has applications in the production of flavoring agents and as an intermediate in organic synthesis. 2-hydroxy-3,5-dimethylbenzaldehyde has a white crystalline appearance and a characteristic almond-like odor. It is considered to be a relatively stable compound under normal conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 24623-61-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,6,2 and 3 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 24623-61:
(7*2)+(6*4)+(5*6)+(4*2)+(3*3)+(2*6)+(1*1)=98
98 % 10 = 8
So 24623-61-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H10O2/c1-6-3-7(2)9(11)8(4-6)5-10/h3-5,11H,1-2H3

24623-61-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-hydroxy-3,5-dimethylbenzaldehyde

1.2 Other means of identification

Product number -
Other names 2-hydroxy-3,5-dimethyl-benzaldehyde

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:24623-61-8 SDS

24623-61-8Relevant articles and documents

Salicylaldimine-aluminum complexes for the facile and efficient ring-opening polymerization of ε-caprolactone

Nomura, Nobuyoshi,Aoyama, Takuji,Ishii, Ryohei,Kondo, Tadao

, p. 5363 - 5366 (2005)

A facile and efficient catalytic system of salicylaldimine-aluminum complexes for the ring-opening polymerization (ROP) of ε-caprolactone (CL) was investigated. The polymerization of Cl was examined at 25 °C in the presence of 1 mol % of benzyl alcohol (B

-

Bamberger,Weiler

, p. 361 (1898)

-

NOVEL SMALL MOLECULE DRUG CONJUGATES OF GEMCITABINE DERIVATIVES

-

Page/Page column 63, (2019/08/26)

Disclosed are compounds having formula (I) or a pharmaceutically acceptable salt, ester, amide, solvate, or stereoisomer thereof, wherein L, Y1, Y2, Y3, Y4, Y5, Z1, Z2, Z3, Z4, Z5, Z6, and Effector are each as defined in the specification; compositions thereof; uses thereof; and methods of use thereof.

A designed protein binding-pocket to control excited-state intramolecular proton transfer fluorescence

Lampkin, Bryan J.,Monteiro, Cecilia,Powers, Evan T.,Bouc, Paige M.,Kelly, Jeffery W.,Vanveller, Brett

supporting information, p. 1076 - 1080 (2019/02/07)

Excited-state intramolecular proton transfer involves a photochemical isomerization and creates the opportunity for the emission of two distinct wavelengths of light from a single fluorophore. The selectivity between these two wavelengths of emission is d

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 24623-61-8