Cas 256382-84-0,(2R,5R)-2-Butyl-1-(toluene-4-sulfonyl)-5-[(Z)-3-(2,5,5-trimethyl-[1,3]dioxan-2-yl)-propenyl]-pyrrolidine

256382-84-0

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Basic information

Product Name: (2R,5R)-2-Butyl-1-(toluene-4-sulfonyl)-5-[(Z)-3-(2,5,5-trimethyl-[1,3]dioxan-2-yl)-propenyl]-pyrrolidine
Synonyms: (2R,5R)-2-Butyl-1-(toluene-4-sulfonyl)-5-[(Z)-3-(2,5,5-trimethyl-[1,3]dioxan-2-yl)-propenyl]-pyrrolidine
CAS NO:256382-84-0
Molecular Formula:
Molecular Weight: 449.655
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: (2R,5R)-2-Butyl-1-(toluene-4-sulfonyl)-5-[(Z)-3-(2,5,5-trimethyl-[1,3]dioxan-2-yl)-propenyl]-pyrrolidine(CAS DataBase Reference)
NIST Chemistry Reference: (2R,5R)-2-Butyl-1-(toluene-4-sulfonyl)-5-[(Z)-3-(2,5,5-trimethyl-[1,3]dioxan-2-yl)-propenyl]-pyrrolidine(256382-84-0)
EPA Substance Registry System: (2R,5R)-2-Butyl-1-(toluene-4-sulfonyl)-5-[(Z)-3-(2,5,5-trimethyl-[1,3]dioxan-2-yl)-propenyl]-pyrrolidine(256382-84-0)

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: 256382-84-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 256382-84-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,6,3,8 and 2 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 256382-84:
(8*2)+(7*5)+(6*6)+(5*3)+(4*8)+(3*2)+(2*8)+(1*4)=160
160 % 10 = 0
So 256382-84-0 is a valid CAS Registry Number.

256382-84-0Upstream product

256382-84-0Downstream Products

256382-85-1 (2R,5S)-2-Butyl-1-(toluene-4-sulfonyl)-5-[3-(2,5,5-trimethyl-[1,3]dioxan-2-yl)-propyl]-pyrrolidine

256382-84-0Relevant academic research and scientific papers

A general approach to indolizidine alkaloids from 1-benzyloxy-5-(p- toluenesulfonamido)-3-alken-2-ols: Synthesis of (+)-monomorine I

Riesinger, Steven W.,L?fstedt, Joakim,Pettersson-Fasth, Helena,B?ckvall, Jan-E.

, p. 3277 - 3280 (2007/10/03)

A versatile method for the preparation of indolizidine alkaloids from 1- benzyloxy-5-(p-toluenesulfonamido)-3-alken-2-ols as stereodefined key intermediates has been developed. The utility of this approach was demonstrated by the synthesis of (+)-monomori

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