Welcome to LookChem.com Sign In|Join Free
  • or
3,4-Dihydro-8-methoxy-2H-1-benzopyran-3-ol, commonly referred to as dihydrokaempferol, is a flavonoid compound characterized by the molecular formula C16H16O4. It is a natural plant pigment and antioxidant that is prevalent in a variety of fruits and vegetables. This chemical is celebrated for its potential health benefits, which encompass anti-inflammatory, antiviral, and antitumor properties. 3,4-Dihydro-8-methoxy-2H-1-benzopyran-3-ol's multifaceted applications in both the pharmaceutical and food industries, particularly in the creation of drugs and functional foods, make it a subject of significant interest for researchers and industry professionals.

91520-01-3

Post Buying Request

91520-01-3 Suppliers

Recommended suppliers

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

91520-01-3 Usage

Uses

Used in Pharmaceutical Industry:
3,4-Dihydro-8-methoxy-2H-1-benzopyran-3-ol is utilized as a key component in drug development for its potential health benefits, such as its anti-inflammatory, antiviral, and antitumor properties. Its presence in formulations can contribute to the management and treatment of various conditions and diseases.
Used in Food Industry:
In the food industry, 3,4-Dihydro-8-methoxy-2H-1-benzopyran-3-ol is employed as an ingredient in the development of functional foods. Its antioxidant properties can enhance the nutritional value of these products, potentially promoting consumer health.
Used in Antioxidant Formulations:
3,4-Dihydro-8-methoxy-2H-1-benzopyran-3-ol is used as an antioxidant in various applications to protect against oxidative stress and related cellular damage, which is beneficial in both medicinal and dietary contexts.
Used in Anti-Inflammatory Agents:
3,4-Dihydro-8-methoxy-2H-1-benzopyran-3-ol serves as an anti-inflammatory agent, making it suitable for treatments aimed at reducing inflammation and associated discomfort or damage.
Used in Antiviral Treatments:
3,4-Dihydro-8-methoxy-2H-1-benzopyran-3-ol is applied as an antiviral agent, potentially inhibiting the replication or infectivity of viruses, thereby contributing to treatments for viral infections.
Used in Antitumor Therapies:
In the realm of oncology, 3,4-Dihydro-8-methoxy-2H-1-benzopyran-3-ol is harnessed for its antitumor properties, possibly aiding in the prevention or mitigation of tumor growth and progression.

Check Digit Verification of cas no

The CAS Registry Mumber 91520-01-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,5,2 and 0 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 91520-01:
(7*9)+(6*1)+(5*5)+(4*2)+(3*0)+(2*0)+(1*1)=103
103 % 10 = 3
So 91520-01-3 is a valid CAS Registry Number.
InChI:InChI=1S/C10H12O3/c1-12-9-4-2-3-7-5-8(11)6-13-10(7)9/h2-4,8,11H,5-6H2,1H3

91520-01-3SDS

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 8-methoxy-3,4-dihydro-2H-chromen-3-ol

1.2 Other means of identification

Product number -
Other names 3,4-dihydro-3-hydroxy-8-methoxy-2H-1-benzopyran

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:91520-01-3 SDS

91520-01-3Relevant academic research and scientific papers

Efficient synthesis of 8-methoxy-3,4-dihydro-2H-1-benzopyran-3-ol

Shindikar,Viswanathan

, p. 1141 - 1145 (2011/05/05)

The article reports a practical, simple, and inexpensive procedure for the synthesis of 8-methoxy-3,4-dihydro-2H-1-benzopyran-3-ol (1). 2-Methoxy phenol on treatment offers the oxirane compound, which undergoes ring cleavage under acidic conditions to give a chlorohydrin, which on acylation and cyclization in the presence of stannic chloride followed by hydrolysis of the acetyl group, yields the desired compound (1).

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 91520-01-3