Cas 351034-16-7,5-[1-Benzo[1,3]dioxol-5-yl-meth-(Z)-ylidene]-2-thioxo-3-p-tolyl-imidazolidin-4-one

351034-16-7

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Basic information

Product Name: 5-[1-Benzo[1,3]dioxol-5-yl-meth-(Z)-ylidene]-2-thioxo-3-p-tolyl-imidazolidin-4-one
Synonyms: 5-[1-Benzo[1,3]dioxol-5-yl-meth-(Z)-ylidene]-2-thioxo-3-p-tolyl-imidazolidin-4-one
CAS NO:351034-16-7
Molecular Formula:
Molecular Weight: 338.387
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 5-[1-Benzo[1,3]dioxol-5-yl-meth-(Z)-ylidene]-2-thioxo-3-p-tolyl-imidazolidin-4-one(CAS DataBase Reference)
NIST Chemistry Reference: 5-[1-Benzo[1,3]dioxol-5-yl-meth-(Z)-ylidene]-2-thioxo-3-p-tolyl-imidazolidin-4-one(351034-16-7)
EPA Substance Registry System: 5-[1-Benzo[1,3]dioxol-5-yl-meth-(Z)-ylidene]-2-thioxo-3-p-tolyl-imidazolidin-4-one(351034-16-7)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 351034-16-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 351034-16-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,1,0,3 and 4 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 351034-16:
(8*3)+(7*5)+(6*1)+(5*0)+(4*3)+(3*4)+(2*1)+(1*6)=97
97 % 10 = 7
So 351034-16-7 is a valid CAS Registry Number.

351034-16-7Upstream product

351034-16-7Downstream Products

351034-16-7Relevant academic research and scientific papers

Glycosylation of 2-thiohydantoin derivatives. Synthesis of some novel S-alkylated and S-glucosylated hydantoins

Khodair, Ahmed I.

, p. 445 - 453 (2007/10/03)

3-Aryl-5-((Z)-arylidene)-3-aryl-2-(2-methylthioethyl)-2-thiohydantoins 3a-f and 3-aryl-5-((Z)-arylidene)-2-(2′,3′,4′,6′-tetra-O- acetyl-β-D-glucopyranosyl)-2-thiohydantoins 7a-n were prepared from the reaction of 3-aryl-5-((Z)-arylidene)-2-thiohydantoins

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