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3-[(2E,4E)-4,6-dimethylocta-2,4-dienoyl]-1,2-dihydroxy-5-(4-hydroxyphenyl)pyridin-4(1H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81844-67-9

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  • 3-[(2E,4E)-4,6-dimethylocta-2,4-dienoyl]-1,2-dihydroxy-5-(4-hydroxyphenyl)pyridin-4(1H)-one

    Cas No: 81844-67-9

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81844-67-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81844-67-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,8,4 and 4 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 81844-67:
(7*8)+(6*1)+(5*8)+(4*4)+(3*4)+(2*6)+(1*7)=149
149 % 10 = 9
So 81844-67-9 is a valid CAS Registry Number.

81844-67-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name tenellin

1.2 Other means of identification

Product number -
Other names Tenellin

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:81844-67-9 SDS

81844-67-9Downstream Products

81844-67-9Relevant articles and documents

Convergent Total Synthesis of (+/-)-Tenellin

Rigby, James H.,Qabar, Maher

, p. 5852 - 5853 (2007/10/02)

A convergent total synthesis of the fungal biochrome tenellin is reported.The synthesis features an efficient cyclocondensation of a cinnamate derived isocyanate with a fully elaborated diene β-keto ester enolate reaction partner.

Synthesis of Racemic Tenellin

Williams, David R.,Sit, Sing-Yuen

, p. 2846 - 2851 (2007/10/02)

Total synthesis of racemic tenellin, a yellow pigment of the insect pathogenic fungus Beauveria, has been accomplished.Preparation of 1,4-dihydroxy-5-(p-hydroxyphenyl)-2(1H)-pyridinone is achieved in excellent overall yield by utilizing an intramolecular C-acylation of an imidazolide precursor.A facile conjugate reduction of the vinylogous amide 6 is illustrated with sodium cyanoborohydride.

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