Cas 326478-83-5,2,6-anhydro-1,3,4-trideoxy-1-[(diphenoxyphosphoryl)amino]-5,7-di-O-methyl-D-arabino-heptitol

326478-83-5

Post Buying Request

Basic information

Product Name: 2,6-anhydro-1,3,4-trideoxy-1-[(diphenoxyphosphoryl)amino]-5,7-di-O-methyl-D-arabino-heptitol
Synonyms: 2,6-anhydro-1,3,4-trideoxy-1-[(diphenoxyphosphoryl)amino]-5,7-di-O-methyl-D-arabino-heptitol
CAS NO:326478-83-5
Molecular Formula:
Molecular Weight: 421.43
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: 2,6-anhydro-1,3,4-trideoxy-1-[(diphenoxyphosphoryl)amino]-5,7-di-O-methyl-D-arabino-heptitol(CAS DataBase Reference)
NIST Chemistry Reference: 2,6-anhydro-1,3,4-trideoxy-1-[(diphenoxyphosphoryl)amino]-5,7-di-O-methyl-D-arabino-heptitol(326478-83-5)
EPA Substance Registry System: 2,6-anhydro-1,3,4-trideoxy-1-[(diphenoxyphosphoryl)amino]-5,7-di-O-methyl-D-arabino-heptitol(326478-83-5)

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: 326478-83-5(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

326478-83-5 Suppliers

Recommended suppliers

326478-83-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 326478-83-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,6,4,7 and 8 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 326478-83:
(8*3)+(7*2)+(6*6)+(5*4)+(4*7)+(3*8)+(2*8)+(1*3)=165
165 % 10 = 5
So 326478-83-5 is a valid CAS Registry Number.

326478-83-5Upstream product

326478-83-5Downstream Products

326478-83-5Relevant academic research and scientific papers

Intramolecular hydrogen abstraction reaction promoted by N-radicals in carbohydrates. Synthesis of chiral 7-oxa-2-azabicyclo[2.2.1]heptane and 8-oxa-6-azabicyclo[3.2.1]octane Ring systems

Francisco, Cosme G.,Herrera, Antonio J.,Suarez, Ernesto

, p. 1012 - 1017 (2003)

The reaction of phenyl and benzyl amidophosphates and alkyl and benzyl carbamate derivatives of aminoalditols with (diacetoxyiodo)benzene or iodosylbenzene and iodine is a mild and selective procedure for the synthesis of chiral 7-oxa-2-azabicyclo[2.2.1]h

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 326478-83-5