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501-16-6

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501-16-6 Usage

Uses

trans-Caffeic Acid is a useful synthetic intermediate. It was used as a reactant to synthesize N-caffeoylphenalkylamide derivatives as bacterial efflux pump inhibitors. It is also used to prepare caffeic acid phenethyl ester analogs with antitumor structures.

Chemical Properties

Pale yellow crystalline powder

General Description

This substance is a primary reference substance with assigned absolute purity (considering chromatographic purity, water, residual solvents, inorganic impurities). The exact value can be found on the certificate. Produced by PhytoLab GmbH & Co. KG

Check Digit Verification of cas no

The CAS Registry Mumber 501-16-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,0 and 1 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 501-16:
(5*5)+(4*0)+(3*1)+(2*1)+(1*6)=36
36 % 10 = 6
So 501-16-6 is a valid CAS Registry Number.

501-16-6 Well-known Company Product Price

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  • Sigma-Aldrich

  • (51868)  trans-Caffeic acid  certified reference material, TraceCERT®

  • 501-16-6

  • 51868-50MG

  • 1,075.23CNY

  • Detail

501-16-6SDS

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 trans-Caffeic acid

1.2 Other means of identification

Product number -
Other names 2-Propenoic acid, 3-(3,4-dihydroxyphenyl)-, (E)-

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:501-16-6 SDS

501-16-6Relevant articles and documents

Detailed mechanism of phenol-inhibited peroxidase-catalyzed oxidation of indole-3-acetic acid at neutral pH

Krylov, Sergey N.,Dunford, H. Brian

, p. 735 - 741 (1996)

The inhibition of horseradish peroxidase (HRP)-catalyzed oxidation of indole-3-acetic acid (IAA) by a phenol, caffeic acid (CA), was studied using both a kinetic approach and computer simulation. The presence of CA resulted in a lag period in IAA oxidation. The lag period increased slowly with increasing [CA] until a critical concentration, [CA]cr, was reached, then it increased much faster when [CA] was greater than [CA]cr The [CA]cr was proportional to [IAA] and did not depend upon [HRP]. Caffeic acid was oxidized by compound I and compound II of HRP with bimolecular rate constants (6.8 ± 107 and 2.1 ± 107 M-1s-1), which were much higher than the corresponding rate constants for IAA oxidation (2.3 ± 103 and 2.0 ±102 M-1s-1). Our experimental data show that CA inhibits IAA oxidation because it is able to compete effectively as a peroxidase substrate. A model based on a detailed mechanism of IAA oxidation was investigated using computer simulation. A rate constant driving nonenzymatic hydroperoxide formation in IAA solution was determined, 3.0 × 10-7 s-1. The model quantitatively describes the experimental results of this work and also qualitatively explains data published earlier. The critical inhibitor concentration is approximately equal to twice the concentration of hydroperoxide in IAA solution at the time of inhibitor addition. Therefore hydroperoxide concentration can be calculated from the determination of critical inhibitor concentration.

Photoinduced Regioselective Olefination of Arenes at Proximal and Distal Sites

Ali, Wajid,Anjana, S. S.,Bhattacharya, Trisha,Chandrashekar, Hediyala B.,Goswami, Nupur,Guin, Srimanta,Maiti, Debabrata,Panda, Sanjib,Prakash, Gaurav,Saha, Argha,Sasmal, Sheuli,Sinha, Soumya Kumar

supporting information, p. 1929 - 1940 (2022/02/01)

The Fujiwara-Moritani reaction has had a profound contribution in the emergence of contemporary C-H activation protocols. Despite the applicability of the traditional approach in different fields, the associated reactivity and regioselectivity issues had

Herbicide based on haloxyfop, flumetsulam and halosulfuron-methyl

-

Paragraph 0038; 0046; 0053; 0061; 0068; 0076, (2021/06/21)

The invention discloses a herbicide based on haloxyfop, flumetsulam and halosulfuron-methyl. The herbicide is prepared from the following raw materials in parts by weight: 1-15 parts of haloxyfop-R-methyl, 1-15 parts of flumetsulam, 1-37 parts of halosulfuron-methyl, 1-2 parts of a modified antioxidant, 10-12 parts of borax, 6-8 parts of a surfactant, 10-12 parts of triethanolamine, 10-12 parts of vegetable oil and 40-42 parts of deionized water. After the haloxyfop-R-methyl, the flumetsulam and the halosulfuron-methyl are mixed, the effects are complementary, the weeding spectrum is wider, the weeding activity is high, the weeding effect is more excellent. In addition, the modified antioxidant is added into the herbicide formula, so that the composite herbicide has the effects of resisting oxidation aging and ultraviolet aging, effective components are prevented from decomposing and losing efficacy in the presence of light, the pesticide effect is kept lasting, and the application prospect and popularization value are remarkably improved.

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