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49821-34-3

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49821-34-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 49821-34-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,8,2 and 1 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 49821-34:
(7*4)+(6*9)+(5*8)+(4*2)+(3*1)+(2*3)+(1*4)=143
143 % 10 = 3
So 49821-34-3 is a valid CAS Registry Number.

49821-34-3SDS

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 (3Z)-3-[(E)-3-(3,4-dimethoxyphenyl)-1-hydroxyprop-2-enylidene]-6-methylpyran-2,4-dione

1.2 Other means of identification

Product number -
Other names -

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:49821-34-3 SDS

49821-34-3Downstream Products

49821-34-3Relevant articles and documents

Synthesis and In vitro Antimicrobial and Antioxidant Screening of Pyrano[4,3-b] Pyrans with Docking Studies

Kamra, Nisha,Kumar, Devinder,Rani, Suman,Singh, Vikramjeet,Thakral, Samridhi,Thakral, Sumit

, p. 457 - 465 (2021/11/24)

The pyrano[4,3-b]pyrans (3a–3j) were synthesized utilizing inexpensive dehydroacetic acid and various sweet-smelling aldehydes in good yield and the structure was elucidated using different spectroscopic techniques. In vitro antimicrobial screening of 3a–

Synthesis of new dihydropyrazoles of designed curcumin analogues

Tripathi, Vishwa Deepak

, p. 1889 - 1894 (2019/08/08)

Present work demonstrates a facile synthesis of a series of 20 dihydropyrazole derivatives from well designed curcumin analogues by reaction of chalcone derivatives with phenylhydrazine. All the synthesized compounds were characterized by spectroscopic (1H and 13C NMR, IR spectra), spectrometric (Mass spectra) data and elemental analysis. Synthesized dihydropyrazoles have diversity points on attached phenyl ring. Effect of substituent on reactivity was explained on the basis of electronic effect generated due to groups on phenyl ring. Presence of dd (double doublet) in 1H NMR spectrum of dihydropyrazoles was also explained due to presence of optically active carbon of pyrazole ring.

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