Cas 155836-68-3,(-)-3-((R)-((2S,5R)-4-allyl-2,5-dimethyl-1-piperazinyl)(4-bromo-2-thienyl)methyl)phenol

155836-68-3

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Basic information

Product Name: (-)-3-((R)-((2S,5R)-4-allyl-2,5-dimethyl-1-piperazinyl)(4-bromo-2-thienyl)methyl)phenol
Synonyms: (-)-3-((R)-((2S,5R)-4-allyl-2,5-dimethyl-1-piperazinyl)(4-bromo-2-thienyl)methyl)phenol
CAS NO:155836-68-3
Molecular Formula:
Molecular Weight: 421.401
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: (-)-3-((R)-((2S,5R)-4-allyl-2,5-dimethyl-1-piperazinyl)(4-bromo-2-thienyl)methyl)phenol(CAS DataBase Reference)
NIST Chemistry Reference: (-)-3-((R)-((2S,5R)-4-allyl-2,5-dimethyl-1-piperazinyl)(4-bromo-2-thienyl)methyl)phenol(155836-68-3)
EPA Substance Registry System: (-)-3-((R)-((2S,5R)-4-allyl-2,5-dimethyl-1-piperazinyl)(4-bromo-2-thienyl)methyl)phenol(155836-68-3)

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: 155836-68-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 155836-68-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,8,3 and 6 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 155836-68:
(8*1)+(7*5)+(6*5)+(5*8)+(4*3)+(3*6)+(2*6)+(1*8)=163
163 % 10 = 3
So 155836-68-3 is a valid CAS Registry Number.

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155836-68-3Relevant academic research and scientific papers

Synthesis, stereochemistry, and opioid receptor binding activity of heterocyclic analogues of BW373U86

Boswell,McNutt,Bubacz,Davis,Chang

, p. 1801 - 1818 (2007/10/03)

The synthesis of a series of heterocyclic analogues of (±)-4-((αR*)-α-((2S*,5R*)-4-allyl-2,5-dimethyl-1-piperazinyl)-3- hydroxybenzyl)-N,N-diethylbenzamide (BW373U86) for screening against opioid receptors is described. The intermediate α-heterocyclic ben

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