Cas 952117-19-0,(R)-(+)-tert-butyl [1-(4-benzyloxy-N-(but-3-en-1-yl)benzamido)but-3-en-2-yl]carbamate

952117-19-0

Post Buying Request

Basic information

Product Name: (R)-(+)-tert-butyl [1-(4-benzyloxy-N-(but-3-en-1-yl)benzamido)but-3-en-2-yl]carbamate
Synonyms: (R)-(+)-tert-butyl [1-(4-benzyloxy-N-(but-3-en-1-yl)benzamido)but-3-en-2-yl]carbamate
CAS NO:952117-19-0
Molecular Formula:
Molecular Weight: 450.578
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)-(+)-tert-butyl [1-(4-benzyloxy-N-(but-3-en-1-yl)benzamido)but-3-en-2-yl]carbamate(CAS DataBase Reference)
NIST Chemistry Reference: (R)-(+)-tert-butyl [1-(4-benzyloxy-N-(but-3-en-1-yl)benzamido)but-3-en-2-yl]carbamate(952117-19-0)
EPA Substance Registry System: (R)-(+)-tert-butyl [1-(4-benzyloxy-N-(but-3-en-1-yl)benzamido)but-3-en-2-yl]carbamate(952117-19-0)

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: 952117-19-0(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

952117-19-0 Suppliers

Recommended suppliers

952117-19-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 952117-19-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,2,1,1 and 7 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 952117-19:
(8*9)+(7*5)+(6*2)+(5*1)+(4*1)+(3*7)+(2*1)+(1*9)=160
160 % 10 = 0
So 952117-19-0 is a valid CAS Registry Number.

952117-19-0Upstream product

952117-19-0Downstream Products

952117-19-0Relevant academic research and scientific papers

Dynamic kinetic asymmetric allylic amination and acyl migration of vinyl aziridines with imido carboxylates

Trost, Barry M.,Fandrick, Daniel R.,Brodmann, Tobias,Stiles, Dylan T.

, p. 6123 - 6125 (2008/09/16)

(Chemical Equation Presented) An atom-economical method has been developed for the preparation of chiral vicinal diamines through a dynamic kinetic asymmetric allylic amination and acyl-group migration of vinyl aziridines with imido carboxylates. Application of the asymmetric transformation enabled the concise synthesis of the azepane core 1 of (+)-balanol and its syn analogue.

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 952117-19-0