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22042-87-1

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22042-87-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22042-87-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,0,4 and 2 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 22042-87:
(7*2)+(6*2)+(5*0)+(4*4)+(3*2)+(2*8)+(1*7)=71
71 % 10 = 1
So 22042-87-1 is a valid CAS Registry Number.
InChI:InChI=1/C4H9N3S/c1-2-3-6-7-4(5)8/h3H,2H2,1H3,(H3,5,7,8)

22042-87-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (propylideneamino)thiourea

1.2 Other means of identification

Product number -
Other names propanaldehyde thiosemicarbazone

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:22042-87-1 SDS

22042-87-1Relevant articles and documents

Monoazo thiazolotriazole disperse dye and preparation method thereof

-

Paragraph 0043; 0044, (2017/10/07)

The invention relates to a monoazo thiazolotriazole disperse dye compound which has a structural formula (I) and disperse dye made from the monoazo thiazolotriazole disperse dye compound. A monoazo thiazolotriazole heterocyclic structure (3N1S) is introdu

A class of potent tyrosinase inhibitors: Alkylidenethiosemicarbazide compounds

Liu, Jinbing,Cao, Rihui,Yi, Wei,Ma, Chunming,Wan, Yiqian,Zhou, Binhua,Ma, Lin,Song, Huacan

experimental part, p. 1773 - 1778 (2009/05/26)

A series of alkylidenethiosemicarbazide compounds were synthesized and their inhibitory effects on the diphenolase activity of mushroom tyrosinase were evaluated. The results showed that most of the synthesized compounds exhibited significant inhibitory activities. Especially, compound 1f was found to be the most potent inhibitor with IC50 value of 0.086 μM, suggesting that further development of such compounds may be of interest.

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