Cas 1237747-29-3,N-((E)-(4-(trifluoromethyl)phenylimino)(morpholino)methyl)-N-(4-(trifluoromethyl)phenyl)morpholine-4-carbothioamide

1237747-29-3

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Basic information

Product Name: N-((E)-(4-(trifluoromethyl)phenylimino)(morpholino)methyl)-N-(4-(trifluoromethyl)phenyl)morpholine-4-carbothioamide
Synonyms:
CAS NO:1237747-29-3
Molecular Formula:
Molecular Weight: 546.537
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: N-((E)-(4-(trifluoromethyl)phenylimino)(morpholino)methyl)-N-(4-(trifluoromethyl)phenyl)morpholine-4-carbothioamide(CAS DataBase Reference)
NIST Chemistry Reference: N-((E)-(4-(trifluoromethyl)phenylimino)(morpholino)methyl)-N-(4-(trifluoromethyl)phenyl)morpholine-4-carbothioamide(1237747-29-3)
EPA Substance Registry System: N-((E)-(4-(trifluoromethyl)phenylimino)(morpholino)methyl)-N-(4-(trifluoromethyl)phenyl)morpholine-4-carbothioamide(1237747-29-3)

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: 1237747-29-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1237747-29-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,7,7,4 and 7 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1237747-29:
(9*1)+(8*2)+(7*3)+(6*7)+(5*7)+(4*4)+(3*7)+(2*2)+(1*9)=173
173 % 10 = 3
So 1237747-29-3 is a valid CAS Registry Number.

1237747-29-3Upstream product

892723-85-2 C₁₂H₁₃F₃N₂OS

1237747-29-3Downstream Products

1237747-29-3Relevant academic research and scientific papers

Arylthioureas with bromine or its equivalents gives no 'Hugerschoff' reaction product

Yella, Ramesh,Murru, Siva,Ali, Abdur Rezzak,Patel, Bhisma K.

experimental part, p. 3389 - 3393 (2010/08/22)

The in situ generated aryl-alkyl unsymmetrical thiourea obtained by the reaction of an aryl isothiocyanate with an aliphatic secondary amine on treatment with bromine or its equivalent gave exclusively a product having a thioamido guanidino moiety and not the expected Hugerschoff product 2-aminobenzothiazole. A plausible reaction mechanism has been proposed for this unprecedented transformation and the scope has been extended to various substrates. The Royal Society of Chemistry 2010.

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