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69964-40-5

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69964-40-5 Usage

Derivative of 2H-chromene

benzopyran compound
2,2-dimethyl-2H-chromene-6-carbaldehyde is derived from the parent compound 2H-chromene, which is a type of benzopyran, a fused bicyclic compound consisting of a benzene ring and a pyran ring.

-6-carbaldehyde suffix

The suffix "-6-carbaldehyde" signifies the presence of an aldehyde functional group (a carbonyl group bonded to a hydrogen atom and an alkyl or aryl group) at the sixth carbon atom of the chromene ring in the compound.

Usage in organic synthesis and medicinal chemistry

2,2-dimethyl-2H-chromene-6-carbaldehyde is commonly used as a precursor in the preparation of various pharmaceuticals and bioactive molecules, making it a valuable building block in the synthesis of complex organic compounds.

Specific properties and applications

The specific properties and applications of 2,2-dimethyl-2H-chromene-6-carbaldehyde depend on its individual characteristics, such as reactivity and stability, as well as how it is used in combination with other chemicals in various chemical reactions and processes.

Check Digit Verification of cas no

The CAS Registry Mumber 69964-40-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,9,6 and 4 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 69964-40:
(7*6)+(6*9)+(5*9)+(4*6)+(3*4)+(2*4)+(1*0)=185
185 % 10 = 5
So 69964-40-5 is a valid CAS Registry Number.

69964-40-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-dimethylchromene-6-carbaldehyde

1.2 Other means of identification

Product number -
Other names 2,2-DIMETHYL-2H-CHROMENE-6-CARBALDEHYDE

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:69964-40-5 SDS

69964-40-5Relevant articles and documents

Flavonoid-triazolyl hybrids as potential anti-hepatitis C virus agents: Synthesis and biological evaluation

Zhang, Han,Zheng, Xin,Li, Jichong,Liu, Qingbo,Huang, Xiao-Xiao,Ding, Huaiwei,Suzuki, Ryosuke,Muramatsu, Masamichi,Song, Shao-Jiang

, (2021/04/12)

A series of flavonoid-triazolyl hybrids were synthesized and evaluated as novel inhibitors of hepatitis C virus (HCV). The results of anti-HCV activity assays showed that most of the synthesized derivatives at a concentration of 100 μg/mL inhibited the ge

Butenolide derivative as well as preparation method and application thereof

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Paragraph 0034-0036; 0038, (2020/07/21)

The invention discloses a butenolide compound as well as a preparation method and an application thereof. The butenolide derivative has the inhibitory activity of protein tyrosine phosphatase 1B (PTP1B), improves insulin resistance of HepG2 cells, generates a remarkable hypoglycemic effect and can be used for preparing a medicine for treating diabetes mellitus.

Synthesis method and use of natural product Angusticornin A

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Paragraph 0005; 0008, (2019/11/21)

The invention discloses a synthesis method and use of a natural product that is Angusticornin A. The structure formula (I) of the natural product is shown in the description. The obtained natural product Angusticornin A has good inhibitory activity agains

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