Cas 1094359-30-4,1-[4,4-dimethyl-1-(toluene-4-sulfonyl)-pyrrolidin-2-ylmethoxy]-2,2,6,6-tetramethyl-piperidine

1094359-30-4

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Basic information

Product Name: 1-[4,4-dimethyl-1-(toluene-4-sulfonyl)-pyrrolidin-2-ylmethoxy]-2,2,6,6-tetramethyl-piperidine
Synonyms: 1-[4,4-dimethyl-1-(toluene-4-sulfonyl)-pyrrolidin-2-ylmethoxy]-2,2,6,6-tetramethyl-piperidine
CAS NO:1094359-30-4
Molecular Formula:
Molecular Weight: 422.632
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: 1-[4,4-dimethyl-1-(toluene-4-sulfonyl)-pyrrolidin-2-ylmethoxy]-2,2,6,6-tetramethyl-piperidine(CAS DataBase Reference)
NIST Chemistry Reference: 1-[4,4-dimethyl-1-(toluene-4-sulfonyl)-pyrrolidin-2-ylmethoxy]-2,2,6,6-tetramethyl-piperidine(1094359-30-4)
EPA Substance Registry System: 1-[4,4-dimethyl-1-(toluene-4-sulfonyl)-pyrrolidin-2-ylmethoxy]-2,2,6,6-tetramethyl-piperidine(1094359-30-4)

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: 1094359-30-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1094359-30-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,4,3,5 and 9 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1094359-30:
(9*1)+(8*0)+(7*9)+(6*4)+(5*3)+(4*5)+(3*9)+(2*3)+(1*0)=164
164 % 10 = 4
So 1094359-30-4 is a valid CAS Registry Number.

1094359-30-4Upstream product

1094359-30-4Downstream Products

212890-85-2 (S)-(+)-(4,4-dimethylpyrrolidin-2-yl)methan-1-ol

1094359-30-4Relevant academic research and scientific papers

Mechanistic analysis and optimization of the copper-catalyzed enantioselective intramolecular alkene aminooxygenation

Paderes, Monissa C.,Keister, Jerome B.,Chemler, Sherry R.

, p. 506 - 515 (2013/02/26)

The catalytic asymmetric aminooxygenation of alkenes provides an efficient and straightforward approach to prepare chiral vicinal amino alcohols. We have reported a copper(II)-catalyzed enantioselective intramolecular alkene aminooxygenation, using (2,2,6

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