Cas 234772-44-2,(R,S)-N-[2-(2-methyl-propyl-1-)]-benzyl-carbonate-2-(N'-methylacetamido)-3-methylbutanamide

234772-44-2

Post Buying Request

Basic information

Product Name: (R,S)-N-[2-(2-methyl-propyl-1-)]-benzyl-carbonate-2-(N'-methylacetamido)-3-methylbutanamide
Synonyms: (R,S)-N-[2-(2-methyl-propyl-1-)]-benzyl-carbonate-2-(N'-methylacetamido)-3-methylbutanamide
CAS NO:234772-44-2
Molecular Formula:
Molecular Weight: 378.469
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: (R,S)-N-[2-(2-methyl-propyl-1-)]-benzyl-carbonate-2-(N'-methylacetamido)-3-methylbutanamide(CAS DataBase Reference)
NIST Chemistry Reference: (R,S)-N-[2-(2-methyl-propyl-1-)]-benzyl-carbonate-2-(N'-methylacetamido)-3-methylbutanamide(234772-44-2)
EPA Substance Registry System: (R,S)-N-[2-(2-methyl-propyl-1-)]-benzyl-carbonate-2-(N'-methylacetamido)-3-methylbutanamide(234772-44-2)

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: 234772-44-2(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

234772-44-2 Suppliers

Recommended suppliers

234772-44-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 234772-44-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,4,7,7 and 2 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 234772-44:
(8*2)+(7*3)+(6*4)+(5*7)+(4*7)+(3*2)+(2*4)+(1*4)=142
142 % 10 = 2
So 234772-44-2 is a valid CAS Registry Number.

234772-44-2Upstream product

234772-44-2Downstream Products

234772-44-2Relevant academic research and scientific papers

A new class of convertible isocyanides in the Ugi four-component reaction

Lindhorst, Thomas,Bock, Holger,Ugi, Ivar

, p. 7411 - 7420 (1999)

The synthesis of a new class of isocyanides and its application in the Ugi reaction is described Ugi products derived from (β-isocyano-ethyl)- alkyl-carbonates can be converted to N-acylated α-amino acids and esters under mild basic conditions.

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 234772-44-2