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104216-97-9

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104216-97-9 Usage

General Description

(2,3,4-Trimethoxyphenyl)acetaldehyde is a chemical compound with the molecular formula C11H14O4. It is a colorless to pale yellow liquid with a strong, pungent odor. (2,3,4-Trimethoxyphenyl)acetaldehyde is commonly used as a fragrance ingredient in perfumes, soaps, and cosmetics. It is also used in the synthesis of pharmaceuticals and other organic compounds. The compound is considered to be a potential irritant and should be handled with caution. Additionally, it is important to note that (2,3,4-Trimethoxyphenyl)acetaldehyde may have toxic effects if ingested or inhaled, so proper safety measures should be taken when working with this chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 104216-97-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,2,1 and 6 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 104216-97:
(8*1)+(7*0)+(6*4)+(5*2)+(4*1)+(3*6)+(2*9)+(1*7)=89
89 % 10 = 9
So 104216-97-9 is a valid CAS Registry Number.

104216-97-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2,3,4-trimethoxyphenyl)acetaldehyde

1.2 Other means of identification

Product number -
Other names 2,3,4-trimethoxyphenylethanal

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:104216-97-9 SDS

104216-97-9Upstream product

104216-97-9Relevant articles and documents

Inhibitors of Dihydrofolate Reductase With Antibacterial Antiprotozoal, Antifungal and Anticancer Properties

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Page/Page column 27, (2009/05/29)

The compositions and methods described herein discloses the design, synthesis and testing of compounds that act as inhibitors of DHFR. The basic scaffold of these inhibitors includes a 2,4-diaminopyrimidine ring with a propargyl linker to another substitu

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