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64700-73-8

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64700-73-8 Usage

Derived from

Metabolism of the amino acid tyrosine

Role

Plays a role in the pathway of the breakdown of tyrosine and phenylalanine

Potential involvement

In certain metabolic disorders such as alkaptonuria

Health issues

Can accumulate and lead to various health issues in alkaptonuria

Research

Suggests antioxidant and anti-inflammatory properties

Interest

In pharmaceutical and medical applications

Significance

Biologically significant compound with potential implications in health and medicine.

Check Digit Verification of cas no

The CAS Registry Mumber 64700-73-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,7,0 and 0 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 64700-73:
(7*6)+(6*4)+(5*7)+(4*0)+(3*0)+(2*7)+(1*3)=118
118 % 10 = 8
So 64700-73-8 is a valid CAS Registry Number.

64700-73-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-dihydroxyphenylacetic acid

1.2 Other means of identification

Product number -
Other names homogentisic acid

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:64700-73-8 SDS

64700-73-8Downstream Products

64700-73-8Relevant articles and documents

Palladium-Catalyzed 2-(Neopentylsulfinyl)aniline Directed C–H Acetoxylation and Alkenylation of Arylacetamides

Barysevich, Maryia V.,Laktsevich-Iskryk, Marharyta V.,Krech, Anastasiya V.,Zhabinskii, Vladimir N.,Khripach, Vladimir A.,Hurski, Alaksiej L.

supporting information, p. 937 - 943 (2020/02/25)

The 2-(neopentylsulfinyl)aniline directing group that promotes rapid palladium-catalyzed C–H acetoxylation and alkenylation of arylacetamides has been developed. The acetoxylation reaches completion within only 40 min at 100 °C and leads to the bis-functionalized products. Alternatively, the reaction can be carried out at room temperature, which is beneficial for sensitive substrates. For the alkenylation, we have developed a protocol in which easily available 1-substituted cyclopropanols were employed as equivalents of vinyl ketones.

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