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121524-09-2

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121524-09-2 Usage

Biochem/physiol Actions

SR58611A is a potent, specific b3 adrenergic receptor agonist. The EC50 for reduction of β3-mediated spontaneous motility in rat distal colon sections is 3.5 nM. Minimal anti-depressant efficacious doses for SR58611A are 0.1-0.3 mpk in rodent models.

Check Digit Verification of cas no

The CAS Registry Mumber 121524-09-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,5,2 and 4 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 121524-09:
(8*1)+(7*2)+(6*1)+(5*5)+(4*2)+(3*4)+(2*0)+(1*9)=82
82 % 10 = 2
So 121524-09-2 is a valid CAS Registry Number.
InChI:InChI=1/C22H26ClNO4.ClH/c1-2-27-22(26)14-28-20-9-7-15-6-8-19(11-17(15)12-20)24-13-21(25)16-4-3-5-18(23)10-16;/h3-5,7,9-10,12,19,21,24-25H,2,6,8,11,13-14H2,1H3;1H/t19-,21-;/m0./s1

121524-09-2 Well-known Company Product Price

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  • Sigma

  • (SML1070)  SR-58611A  ≥98% (HPLC)

  • 121524-09-2

  • SML1070-5MG

  • 1,107.99CNY

  • Detail
  • Sigma

  • (SML1070)  SR-58611A  ≥98% (HPLC)

  • 121524-09-2

  • SML1070-25MG

  • 4,469.40CNY

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121524-09-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-[[(7S)-7-[[(2R)-2-(3-chlorophenyl)-2-hydroxyethyl]amino]-5,6,7,8-tetrahydronaphthalen-2-yl]oxy]acetate,hydrochloride

1.2 Other means of identification

Product number -
Other names C22H26ClNO4.HCl

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
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More Details:121524-09-2 SDS

121524-09-2Downstream Products

121524-09-2Relevant articles and documents

Alternative synthesis of the chiral atypical β-adrenergic phenylethanolaminotetraline agonist SR58611A using enantioselective hydrogenation

Devocelle, Marc,Mortreux, Andre,Agbossou, Francine,Dormoy, Jean-Robert

, p. 4551 - 4554 (1999)

We have developed an alternative synthesis of the atypical β-adrenergic phenylethanolaminotetraline agonist SR58611A. Two key intermediates have been synthesised involving enantioselective hydrogenation of an aminoketone and an enamide providing the corre

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