Cas 73516-67-3,Cyclopent[e]-1,3-oxazin-2(3H)-one, hexahydro-4-methyl-, (4-alpha-,4a-ba-,7a-ba-)- (9CI)

73516-67-3

Post Buying Request

Basic information

Product Name: Cyclopent[e]-1,3-oxazin-2(3H)-one, hexahydro-4-methyl-, (4-alpha-,4a-ba-,7a-ba-)- (9CI)
Synonyms: Cyclopent[e]-1,3-oxazin-2(3H)-one,hexahydro-4-methyl-,(4-alpha-,4a-bta-,7a-bta-)-(9CI);Cyclopent[e]-1,3-oxazin-2(3H)-one, hexahydro-4-methyl-, (4-alpha-,4a-ba-,7a-ba-)- (9CI)
CAS NO:73516-67-3
Molecular Formula: C8H13NO2
Molecular Weight: 155.19432
EINECS: N/A
Product Categories: CYCLOPENTANE
Mol File: 73516-67-3.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: Cyclopent[e]-1,3-oxazin-2(3H)-one, hexahydro-4-methyl-, (4-alpha-,4a-ba-,7a-ba-)- (9CI)(CAS DataBase Reference)
NIST Chemistry Reference: Cyclopent[e]-1,3-oxazin-2(3H)-one, hexahydro-4-methyl-, (4-alpha-,4a-ba-,7a-ba-)- (9CI)(73516-67-3)
EPA Substance Registry System: Cyclopent[e]-1,3-oxazin-2(3H)-one, hexahydro-4-methyl-, (4-alpha-,4a-ba-,7a-ba-)- (9CI)(73516-67-3)

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: 73516-67-3(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

73516-67-3 Suppliers

Recommended suppliers

73516-67-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73516-67-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,5,1 and 6 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 73516-67:
(7*7)+(6*3)+(5*5)+(4*1)+(3*6)+(2*6)+(1*7)=133
133 % 10 = 3
So 73516-67-3 is a valid CAS Registry Number.

73516-67-3Upstream product

73516-67-3Downstream Products

73516-67-3Relevant academic research and scientific papers

Syntheses via Isoxazolines, 6. - Asymmetric Induction in the Reduction of 2-Isoxazolines to Yield γ-Amino Alcohols with Two or Three Vicinal Stereocentres

Jaeger, Volker,Buss, Volker,Schwab, Wilfried

, p. 122 - 139 (2007/10/02)

The substituted 3-aminopropanols 3 and 5 with two or three adjacent chiral centres are prepared from alkenes and nitrile oxides via LiAlH4 reduction of intermediate isoxazolines 2 and 4, respectively, in a regio- and stereoselective mode. 4-Alkyl groups g

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 73516-67-3