Cas 207922-87-0,N-methyl 4-(2-(2-(2-acetylaminopyridin-5-yl)-2-(R)-hydroxyethyl-N-tert-butyloxycarbonylamino)-ethoxy)-phenylacetamide

207922-87-0

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Basic information

Product Name: N-methyl 4-(2-(2-(2-acetylaminopyridin-5-yl)-2-(R)-hydroxyethyl-N-tert-butyloxycarbonylamino)-ethoxy)-phenylacetamide
Synonyms:
CAS NO:207922-87-0
Molecular Formula:
Molecular Weight: 486.568
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-methyl 4-(2-(2-(2-acetylaminopyridin-5-yl)-2-(R)-hydroxyethyl-N-tert-butyloxycarbonylamino)-ethoxy)-phenylacetamide(CAS DataBase Reference)
NIST Chemistry Reference: N-methyl 4-(2-(2-(2-acetylaminopyridin-5-yl)-2-(R)-hydroxyethyl-N-tert-butyloxycarbonylamino)-ethoxy)-phenylacetamide(207922-87-0)
EPA Substance Registry System: N-methyl 4-(2-(2-(2-acetylaminopyridin-5-yl)-2-(R)-hydroxyethyl-N-tert-butyloxycarbonylamino)-ethoxy)-phenylacetamide(207922-87-0)

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: 207922-87-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 207922-87-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,7,9,2 and 2 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 207922-87:
(8*2)+(7*0)+(6*7)+(5*9)+(4*2)+(3*2)+(2*8)+(1*7)=140
140 % 10 = 0
So 207922-87-0 is a valid CAS Registry Number.

207922-87-0Upstream product

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207922-87-0Relevant academic research and scientific papers

Process research and scale-up for a β-3 adrenergic receptor agonist

Vanderplas, Brian C.,Devries, Keith M.,Fox, Darrell E.,Raggon, Jeffrey W.,Snyder, Michael W.,Urban, Frank J.

, p. 583 - 586 (2004)

A scaleable synthesis of the β-3 adrenergic receptor agonist, (4-{2-[2-(6-aminopyridin-3-yl)-(2R)-hydroxy-ethylamino]ethoxy}-phenyl)acetic acid is presented. The key coupling step utilizes a silyl-protected β-hydroxy tosylate to alkylate a primary amine,

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