Cas 360570-01-0,3-Hydroxy-2-[(S)-2-[(naphthalene-1-carbonyl)-amino]-3-(4-nitro-phenyl)-propionylamino]-propionic acid ethyl ester

360570-01-0

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Basic information

Product Name: 3-Hydroxy-2-[(S)-2-[(naphthalene-1-carbonyl)-amino]-3-(4-nitro-phenyl)-propionylamino]-propionic acid ethyl ester
Synonyms:
CAS NO:360570-01-0
Molecular Formula:
Molecular Weight: 479.489
EINECS: N/A
Product Categories: N/A
Mol File: 360570-01-0.mol
Article Data: 1

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-Hydroxy-2-[(S)-2-[(naphthalene-1-carbonyl)-amino]-3-(4-nitro-phenyl)-propionylamino]-propionic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 3-Hydroxy-2-[(S)-2-[(naphthalene-1-carbonyl)-amino]-3-(4-nitro-phenyl)-propionylamino]-propionic acid ethyl ester(360570-01-0)
EPA Substance Registry System: 3-Hydroxy-2-[(S)-2-[(naphthalene-1-carbonyl)-amino]-3-(4-nitro-phenyl)-propionylamino]-propionic acid ethyl ester(360570-01-0)

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: 360570-01-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 360570-01-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,6,0,5,7 and 0 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 360570-01:
(8*3)+(7*6)+(6*0)+(5*5)+(4*7)+(3*0)+(2*0)+(1*1)=120
120 % 10 = 0
So 360570-01-0 is a valid CAS Registry Number.

360570-01-0Upstream product

39978-59-1 ethyl 2-amino-3-hydroxypropanoate

360570-01-0Downstream Products

360569-78-4 2-[(S)-1-[(Naphthalene-1-carbonyl)-amino]-2-(4-nitro-phenyl)-ethyl]-4,5-dihydro-oxazole-4-carboxylic acid ethyl ester

360570-01-0Relevant articles and documents

Discovery of potent and selective phenylalanine derived CCR3 receptor antagonists. Part 2

Dhanak, Dashyant,Christmann, Lisa T,Darcy, Michael G,Keenan, Richard M,Knight, Steven D,Lee, Judithann,Ridgers, Lance H,Sarau, Henry M,Shah, Dinubhai H,White, John R,Zhang, Lily

, p. 1445 - 1450 (2007/10/03)

Highly potent CCR3 antagonists have been developed from a previously reported series of phenylalanine ester-based leads. Solution-phase, parallel synthesis optimization was utilized to identify highly potent, functional CCR3 antagonists.

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