Cas 1185751-63-6,2-bromo-3-phenyl-2,3-dihydrothiazolo[3,2-a]quinolinium bromide

1185751-63-6

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Basic information

Product Name: 2-bromo-3-phenyl-2,3-dihydrothiazolo[3,2-a]quinolinium bromide
Synonyms: 2-bromo-3-phenyl-2,3-dihydrothiazolo[3,2-a]quinolinium bromide
CAS NO:1185751-63-6
Molecular Formula:
Molecular Weight: 423.171
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: 2-bromo-3-phenyl-2,3-dihydrothiazolo[3,2-a]quinolinium bromide(CAS DataBase Reference)
NIST Chemistry Reference: 2-bromo-3-phenyl-2,3-dihydrothiazolo[3,2-a]quinolinium bromide(1185751-63-6)
EPA Substance Registry System: 2-bromo-3-phenyl-2,3-dihydrothiazolo[3,2-a]quinolinium bromide(1185751-63-6)

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: 1185751-63-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1185751-63-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,8,5,7,5 and 1 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1185751-63:
(9*1)+(8*1)+(7*8)+(6*5)+(5*7)+(4*5)+(3*1)+(2*6)+(1*3)=176
176 % 10 = 6
So 1185751-63-6 is a valid CAS Registry Number.

1185751-63-6Upstream product

127139-66-6 cis-2-styrylthioquinoline

1185751-63-6Downstream Products

1185751-63-6Relevant academic research and scientific papers

Synthesis and halocyclization of 2-alkenylthioquinolines

Kim

, p. 1355 - 1358 (2008)

Bromination of 2-vinylthioquinoline and cis-2-styrylthioquinoline with molecular bromine leads to the formation of 2-bromo(3-phenyl)-2,3- dihydrothiazolo[3,2-a]quinolinium bromides, and of 2-allyl-thioquinoline to a mixture of 2-and 3-bromomethyl-2,3-dihydrothiazolo[3,2-a]quinolinium bromides. Iodine reacts with allylthioquinoline with the formation of 3-iodomethyl-2,3- dihydrothiazolo-[3,2-a]quinolinium triiodide.

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