Cas 3585-72-6,4-(Cyclopentyloxy)-benzeneacetic acid

3585-72-6

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Basic information

Product Name: 4-(Cyclopentyloxy)-benzeneacetic acid
Synonyms: 4-(Cyclopentyloxy)-benzeneacetic acid;(4-Cyclopentyloxy-phenyl)-acetic acid
CAS NO:3585-72-6
Molecular Formula: C₁₃H₁₆O₃
Molecular Weight: 220.26434
EINECS: N/A
Product Categories: N/A
Mol File: 3585-72-6.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 4-(Cyclopentyloxy)-benzeneacetic acid(CAS DataBase Reference)
NIST Chemistry Reference: 4-(Cyclopentyloxy)-benzeneacetic acid(3585-72-6)
EPA Substance Registry System: 4-(Cyclopentyloxy)-benzeneacetic acid(3585-72-6)

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: 3585-72-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 3585-72-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,8 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3585-72:
(6*3)+(5*5)+(4*8)+(3*5)+(2*7)+(1*2)=106
106 % 10 = 6
So 3585-72-6 is a valid CAS Registry Number.

3585-72-6Upstream product

1046140-43-5 C₁₄H₁₈O₃

3585-72-6Downstream Products

3585-72-6Relevant academic research and scientific papers

Novel benzimidazole derivatives as selective CB2 agonists

Pagé, Daniel,Balaux, Elise,Boisvert, Luc,Liu, Ziping,Milburn, Claire,Tremblay, Maxime,Wei, Zhongyong,Woo, Simon,Luo, Xuehong,Cheng, Yun-Xing,Yang, Hua,Srivastava, Sanjay,Zhou, Fei,Brown, William,Tomaszewski, Miroslaw,Walpole, Christopher,Hodzic, Leila,St-Onge, Stéphane,Godbout, Claude,Salois, Dominic,Payza, Keymal

scheme or table, p. 3695 - 3700 (2009/04/04)

The preparation and evaluation of a novel class of CB2 agonists based on a benzimidazole moiety are reported. They showed binding affinities up to 1 nM towards the CB2 receptor with partial to full agonist potencies. They also demonstrated good to excellent selectivity (>1000-fold) over the CB1 receptor.

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