Cas 207985-87-3,3-[(S)-3-((S)-4-Benzyl-2-oxo-oxazolidin-3-yl)-2-hydroxy-3-oxo-propyl]-benzonitrile

207985-87-3

Post Buying Request

Basic information

Product Name: 3-[(S)-3-((S)-4-Benzyl-2-oxo-oxazolidin-3-yl)-2-hydroxy-3-oxo-propyl]-benzonitrile
Synonyms: 3-[(S)-3-((S)-4-Benzyl-2-oxo-oxazolidin-3-yl)-2-hydroxy-3-oxo-propyl]-benzonitrile
CAS NO:207985-87-3
Molecular Formula:
Molecular Weight: 350.374
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-[(S)-3-((S)-4-Benzyl-2-oxo-oxazolidin-3-yl)-2-hydroxy-3-oxo-propyl]-benzonitrile(CAS DataBase Reference)
NIST Chemistry Reference: 3-[(S)-3-((S)-4-Benzyl-2-oxo-oxazolidin-3-yl)-2-hydroxy-3-oxo-propyl]-benzonitrile(207985-87-3)
EPA Substance Registry System: 3-[(S)-3-((S)-4-Benzyl-2-oxo-oxazolidin-3-yl)-2-hydroxy-3-oxo-propyl]-benzonitrile(207985-87-3)

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: 207985-87-3(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

207985-87-3 Suppliers

Recommended suppliers

207985-87-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 207985-87-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,7,9,8 and 5 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 207985-87:
(8*2)+(7*0)+(6*7)+(5*9)+(4*8)+(3*5)+(2*8)+(1*7)=173
173 % 10 = 3
So 207985-87-3 is a valid CAS Registry Number.

207985-87-3Upstream product

207985-87-3Downstream Products

207985-88-4 (S)-3-(3-Cyano-phenyl)-2-hydroxy-propionic acid methyl ester

207985-87-3Relevant academic research and scientific papers

Macrocyclic inhibitors of penicillopepsin. 3. Design, synthesis and evaluation of an inhibitor bridged between P2 and P1'

Smith, Whitney W.,Bartlett, Paul A.

, p. 4622 - 4628 (2007/10/03)

Through application of a thorough design and modeling protocol, the macrocyclic peptidyl phosphonate 5 was derived from the bound structure of an acyclic inhibitor of penicillopepsin, 4, by linking the P1' and P2 side chains; the acyclic analogues 6 and 7

Post a RFQ

Cas No.:

Product Name:

Quantity:

Email:

Company name:

Valid Period:

Detailed Requirements:

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

What can I do for you?
Get Best Price

Get Best Price for 207985-87-3