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74794-91-5

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74794-91-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74794-91-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,7,9 and 4 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 74794-91:
(7*7)+(6*4)+(5*7)+(4*9)+(3*4)+(2*9)+(1*1)=175
175 % 10 = 5
So 74794-91-5 is a valid CAS Registry Number.

74794-91-5SDS

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 (E)-5-(but-2-en-2-yl)-2,2-dimethylfuran-3(2H)-one

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:74794-91-5 SDS

74794-91-5Relevant articles and documents

Dimethoxyindoles based thiosemicarbazones as multi-target agents; synthesis, crystal interactions, biological activity and molecular modeling

Bingul, Murat,Boga, Mehmet,Kandemir, Hakan,Koca, Mehmet Serdar,Saglam, Mehmet F.,Sengul, Ibrahim F.,Temel, Mutesir,Zorlu, Yunus,Y?ld?z, Minhal

, (2022/02/03)

Alzheimer's disease (AD) is known as one of the most devastating neurodegenerative disease diagnosed for the old-aged people and cholinesterase inhibitors (ChEI) can be used as an effective palliative treatment for AD. A range of novel monomeric and dimer

Investigation of the Bischler Indole Synthesis from 3,5-Dimethoxyaniline

Black, David St.C.,Gatehouse, Bryan M.K.C.,Theobald, Francois,Wong, Laurence C.H.

, p. 343 - 350 (2007/10/02)

Cyclization of the amino ketones (3a,b) derived from 3,5-dimethoxyaniline, and phenacyl bromide and 4-bromophenacyl bromide respectively, afforded 2-arylindoles (8a,b) in preference to 3-arylindoles (7).The 3-(4'bromophenyl)indole (7b) was also isolated i

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