Cas 1052676-87-5,benzyl ((4S,5R,6R)-4-tert-butoxy-7-oxo-1-azabicyclo[3.2.0]heptan-6-yl)methylcarbamate

1052676-87-5

Post Buying Request

Basic information

Product Name: benzyl ((4S,5R,6R)-4-tert-butoxy-7-oxo-1-azabicyclo[3.2.0]heptan-6-yl)methylcarbamate
Synonyms: benzyl ((4S,5R,6R)-4-tert-butoxy-7-oxo-1-azabicyclo[3.2.0]heptan-6-yl)methylcarbamate
CAS NO:1052676-87-5
Molecular Formula:
Molecular Weight: 346.426
EINECS: N/A
Product Categories: N/A
Mol File: 1052676-87-5.mol
Article Data: 1

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: benzyl ((4S,5R,6R)-4-tert-butoxy-7-oxo-1-azabicyclo[3.2.0]heptan-6-yl)methylcarbamate(CAS DataBase Reference)
NIST Chemistry Reference: benzyl ((4S,5R,6R)-4-tert-butoxy-7-oxo-1-azabicyclo[3.2.0]heptan-6-yl)methylcarbamate(1052676-87-5)
EPA Substance Registry System: benzyl ((4S,5R,6R)-4-tert-butoxy-7-oxo-1-azabicyclo[3.2.0]heptan-6-yl)methylcarbamate(1052676-87-5)

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: 1052676-87-5(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

1052676-87-5 Suppliers

Recommended suppliersmore

1052676-87-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1052676-87-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,5,2,6,7 and 6 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1052676-87:
(9*1)+(8*0)+(7*5)+(6*2)+(5*6)+(4*7)+(3*6)+(2*8)+(1*7)=155
155 % 10 = 5
So 1052676-87-5 is a valid CAS Registry Number.

1052676-87-5Upstream product

1052676-87-5Downstream Products

1052676-87-5Relevant articles and documents

Diastereoselective synthesis of carbapenams via Kinugasa reaction

Stecko, Sebastian,Mames, Adam,Furman, Bartlomiej,Chmielewski, Marek

supporting information; experimental part, p. 7402 - 7404 (2009/05/07)

(Chemical Equation Presented) A facile approach to carbapenams via Kinugasa reaction between terminal copper acetylides and nonracemic cyclic nitrones derived from malic and tartaric acid is reported. The stereochemical preferences observed in these reactions are explained. The reaction provides an entry to the carbapenams basic skeleton.

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 1052676-87-5