Cas 724772-70-7,<i>N</i>-[4-iodo-2-(2-oxo-4-phenyl-oxazolidine-3-carbonyl)-1-<i>p</i>-tolyl-butyl]-benzenesulfonamide

724772-70-7

Post Buying Request

Basic information

Product Name: N-[4-iodo-2-(2-oxo-4-phenyl-oxazolidine-3-carbonyl)-1-p-tolyl-butyl]-benzenesulfonamide
Synonyms: N-[4-iodo-2-(2-oxo-4-phenyl-oxazolidine-3-carbonyl)-1-p-tolyl-butyl]-benzenesulfonamide
CAS NO:724772-70-7
Molecular Formula:
Molecular Weight: 618.492
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-[4-iodo-2-(2-oxo-4-phenyl-oxazolidine-3-carbonyl)-1-p-tolyl-butyl]-benzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: N-[4-iodo-2-(2-oxo-4-phenyl-oxazolidine-3-carbonyl)-1-p-tolyl-butyl]-benzenesulfonamide(724772-70-7)
EPA Substance Registry System: N-[4-iodo-2-(2-oxo-4-phenyl-oxazolidine-3-carbonyl)-1-p-tolyl-butyl]-benzenesulfonamide(724772-70-7)

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: 724772-70-7(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

724772-70-7 Suppliers

Recommended suppliers

724772-70-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 724772-70-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,2,4,7,7 and 2 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 724772-70:
(8*7)+(7*2)+(6*4)+(5*7)+(4*7)+(3*2)+(2*7)+(1*0)=177
177 % 10 = 7
So 724772-70-7 is a valid CAS Registry Number.

724772-70-7Upstream product

24865-82-5 N-(4-methylbenzylidene)benzenesulfonamide

724772-70-7Downstream Products

724772-71-8 (S)-3-((2S,3R)-1-Benzenesulfonyl-2-p-tolyl-pyrrolidine-3-carbonyl)-4-phenyl-oxazolidin-2-one

724772-70-7Relevant academic research and scientific papers

Asymmetric halo-Mannich-type reaction provides access to pyrrolidines and β-proline derivatives

Timmons, Cody,Guo, Li,Liu, Junying,Cannon, John F.,Li, Guigen

, p. 7634 - 7639 (2007/10/03)

A new halo-Mannich-type reaction is reported using cyclopropyl carbonyl-derived enolates and sulfonyl-protected imines. Chiral oxazolidinones auxiliaries were found to be effective for completely controlling the stereochemistry of the products. Variations

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 724772-70-7