Cas 1533400-55-3,(4S)-4-benzyl-3-(2-(2,8-dimethyl-6,12-dihydro-5,11-methanodibenzo[b,f][1,5]diazocin-13-yl)acetyl)oxazolidin-2-one

1533400-55-3

Post Buying Request

Basic information

Product Name: (4S)-4-benzyl-3-(2-(2,8-dimethyl-6,12-dihydro-5,11-methanodibenzo[b,f][1,5]diazocin-13-yl)acetyl)oxazolidin-2-one
Synonyms:
CAS NO:1533400-55-3
Molecular Formula:
Molecular Weight: 467.568
EINECS: N/A
Product Categories: N/A
Mol File: 1533400-55-3.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: (4S)-4-benzyl-3-(2-(2,8-dimethyl-6,12-dihydro-5,11-methanodibenzo[b,f][1,5]diazocin-13-yl)acetyl)oxazolidin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (4S)-4-benzyl-3-(2-(2,8-dimethyl-6,12-dihydro-5,11-methanodibenzo[b,f][1,5]diazocin-13-yl)acetyl)oxazolidin-2-one(1533400-55-3)
EPA Substance Registry System: (4S)-4-benzyl-3-(2-(2,8-dimethyl-6,12-dihydro-5,11-methanodibenzo[b,f][1,5]diazocin-13-yl)acetyl)oxazolidin-2-one(1533400-55-3)

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: 1533400-55-3(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

1533400-55-3 Suppliers

Recommended suppliersmore

1533400-55-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1533400-55-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,3,3,4,0 and 0 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1533400-55:
(9*1)+(8*5)+(7*3)+(6*3)+(5*4)+(4*0)+(3*0)+(2*5)+(1*5)=123
123 % 10 = 3
So 1533400-55-3 is a valid CAS Registry Number.

1533400-55-3Upstream product

1533400-55-3Downstream Products

1533400-55-3Relevant articles and documents

Asymmetric synthesis of N-stereogenic molecules: Diastereoselective double aza-Michael reaction

Lauber, Alex,Zelenay, Benjamin,Cvengros, Jan

supporting information, p. 1195 - 1197 (2014/02/14)

A novel approach towards the asymmetric synthesis of N-stereogenic molecules via double aza-Michael addition was developed. The diastereomeric ratio can be increased by a thermodynamically controlled isomerization mechanism. Simple separation and functionalization of the products afford N-stereogenic compounds in high enantiomeric purity.

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 1533400-55-3