Cas 596113-51-8,Benzenesulfonic acid, 4-nitro-, (1S)-1-[bis(1-methylethoxy)phosphinyl]propyl ester

596113-51-8

Post Buying Request

Basic information

Product Name: Benzenesulfonic acid, 4-nitro-, (1S)-1-[bis(1-methylethoxy)phosphinyl]propyl ester
Synonyms:
CAS NO:596113-51-8
Molecular Formula: C15H24NO8PS
Molecular Weight: 409.397
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: Benzenesulfonic acid, 4-nitro-, (1S)-1-[bis(1-methylethoxy)phosphinyl]propyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Benzenesulfonic acid, 4-nitro-, (1S)-1-[bis(1-methylethoxy)phosphinyl]propyl ester(596113-51-8)
EPA Substance Registry System: Benzenesulfonic acid, 4-nitro-, (1S)-1-[bis(1-methylethoxy)phosphinyl]propyl ester(596113-51-8)

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: 596113-51-8(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

596113-51-8 Suppliers

Recommended suppliers

596113-51-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 596113-51-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,9,6,1,1 and 3 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 596113-51:
(8*5)+(7*9)+(6*6)+(5*1)+(4*1)+(3*3)+(2*5)+(1*1)=168
168 % 10 = 8
So 596113-51-8 is a valid CAS Registry Number.

596113-51-8Upstream product

596113-51-8Downstream Products

596113-51-8Relevant academic research and scientific papers

Synthesis of chiral, nonracemic α-sulfanylphosphonates and derivatives

Gulea, Mihaela,Hammerschmidt, Friedrich,Marchand, Patrice,Masson, Serge,Pisljagic, Violeta,Wuggenig, Frank

, p. 1829 - 1836 (2003)

Optically active α-sulfanylphosphonates and the corresponding methyl sulfides were prepared in three steps starting from chiral, nonracemic (ee 93-97%) α-hydroxyphosphonates obtained by enzymatic resolution. Reaction conditions for the reduction of racemi

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 596113-51-8