Cas 183204-13-9,Adamantane-1-carboxylic acid {(R)-1-[2-(2-oxo-2-phenyl-ethanesulfonyl)-phenyl]-ethyl}-amide

183204-13-9

Post Buying Request

Basic information

Product Name: Adamantane-1-carboxylic acid {(R)-1-[2-(2-oxo-2-phenyl-ethanesulfonyl)-phenyl]-ethyl}-amide
Synonyms:
CAS NO:183204-13-9
Molecular Formula:
Molecular Weight: 465.613
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: Adamantane-1-carboxylic acid {(R)-1-[2-(2-oxo-2-phenyl-ethanesulfonyl)-phenyl]-ethyl}-amide(CAS DataBase Reference)
NIST Chemistry Reference: Adamantane-1-carboxylic acid {(R)-1-[2-(2-oxo-2-phenyl-ethanesulfonyl)-phenyl]-ethyl}-amide(183204-13-9)
EPA Substance Registry System: Adamantane-1-carboxylic acid {(R)-1-[2-(2-oxo-2-phenyl-ethanesulfonyl)-phenyl]-ethyl}-amide(183204-13-9)

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: 183204-13-9(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

183204-13-9 Suppliers

Recommended suppliers

183204-13-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 183204-13-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,3,2,0 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 183204-13:
(8*1)+(7*8)+(6*3)+(5*2)+(4*0)+(3*4)+(2*1)+(1*3)=109
109 % 10 = 9
So 183204-13-9 is a valid CAS Registry Number.

183204-13-9Upstream product

183204-13-9Downstream Products

183204-13-9Relevant academic research and scientific papers

Asymmetric synthesis of β-hydroxy sulfones by reduction of chiral β-keto sulfones

Bernabeu, M. Carmen,Bonete, Pedro,Caturla, Francisco,Chinchilla, Rafael,Najera, Carmen

, p. 2475 - 2478 (1996)

Chiral β-keto sulfones 3 have been prepared from enantiomerically pure sulfinic acids 2 derived from (R)- and (S)-methylbenzylamine. Enantiospecific reduction of these ketosulfones 3 can be achieved using different hydrides affording β-hydroxy sulfones. O

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 183204-13-9