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83104-76-1

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83104-76-1 Usage

Chemical Family

Belongs to the catecholamine family

Formation

Formed through the oxidation of N-acetyldopamine

Precursor

Acts as a precursor to the pigment melanin

Biological Activities

Exhibits antioxidant, anti-inflammatory, and antibacterial properties

Medical Applications

Potential use in the treatment of neurodegenerative diseases such as Parkinson's and Alzheimer's

Cosmetic Applications

Potential ingredient in cosmetics and skin care products due to its ability to protect the skin from UV radiation and oxidative stress

Check Digit Verification of cas no

The CAS Registry Mumber 83104-76-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,1,0 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 83104-76:
(7*8)+(6*3)+(5*1)+(4*0)+(3*4)+(2*7)+(1*6)=111
111 % 10 = 1
So 83104-76-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H11NO3/c1-7(12)11-5-4-8-2-3-9(13)10(14)6-8/h2-6,13-14H,1H3,(H,11,12)/b5-4+

83104-76-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[(E)-2-(3,4-dihydroxyphenyl)ethenyl]acetamide

1.2 Other means of identification

Product number -
Other names N-Acetyl-1,2-didehydrodopamine

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:83104-76-1 SDS

83104-76-1Downstream Products

83104-76-1Relevant articles and documents

Synthesis of N-Acetyl-1,2-didehydrodopamine. A Key Intermediate Involved in Sclerotization of Insect Cuticule

Ramamurthy, B.,Sugumaran, M.

, p. 523 - 524 (2007/10/02)

The synthesis of N-acetyl-1,2-didehydrodopamine (6; N-acetyl-3,4-dihydroxystyrylamine) was accomplished by demethylation of N-acetyl-3,4-dimethoxystyrylamine (5), formed by sequential treatment of 3,4-dimethoxycinnamic acid (1) with thionyl chloride, sodi

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