Cas 128252-51-7,((S)-2-Methoxymethyl-pyrrolidin-1-yl)-(2-oxa-3-aza-bicyclo[2.2.2]oct-5-en-3-yl)-methanone

128252-51-7

Post Buying Request

Basic information

Product Name: ((S)-2-Methoxymethyl-pyrrolidin-1-yl)-(2-oxa-3-aza-bicyclo[2.2.2]oct-5-en-3-yl)-methanone
Synonyms:
CAS NO:128252-51-7
Molecular Formula:
Molecular Weight: 252.313
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: ((S)-2-Methoxymethyl-pyrrolidin-1-yl)-(2-oxa-3-aza-bicyclo[2.2.2]oct-5-en-3-yl)-methanone(CAS DataBase Reference)
NIST Chemistry Reference: ((S)-2-Methoxymethyl-pyrrolidin-1-yl)-(2-oxa-3-aza-bicyclo[2.2.2]oct-5-en-3-yl)-methanone(128252-51-7)
EPA Substance Registry System: ((S)-2-Methoxymethyl-pyrrolidin-1-yl)-(2-oxa-3-aza-bicyclo[2.2.2]oct-5-en-3-yl)-methanone(128252-51-7)

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: 128252-51-7(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

128252-51-7 Suppliers

Recommended suppliers

128252-51-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 128252-51-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,2,5 and 2 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 128252-51:
(8*1)+(7*2)+(6*8)+(5*2)+(4*5)+(3*2)+(2*5)+(1*1)=117
117 % 10 = 7
So 128252-51-7 is a valid CAS Registry Number.

128252-51-7Upstream product

63126-47-6 (2S)-2-(methoxymethyl)-1-pyrrolidine

128252-51-7Downstream Products

128252-51-7Relevant academic research and scientific papers

Asymmetric Diels-Alder cycloadditions with acylnitroso dienophiles obtained from L-proline

Brouillard-Poichet,Defoin,Streith

, p. 7061 - 7064 (1989)

N-acylnitroso derivatives of L-proline were formed in situ from the corresponding hydroxamic acids. They reacted easily with 1,3-cyclohexadiene to give the corresponding diastereoisomeric pairs of Diels-Alder cycloadducts with d.e. values ranging from 52 to 68%.

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 128252-51-7