Cas 305838-46-4,Dibenzyl-[(1S,2R)-1-(tert-butyl-dimethyl-silanyloxymethyl)-4-[1,3]dioxolan-2-yl-2-methoxymethoxy-butyl]-amine

305838-46-4

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Basic information

Product Name: Dibenzyl-[(1S,2R)-1-(tert-butyl-dimethyl-silanyloxymethyl)-4-[1,3]dioxolan-2-yl-2-methoxymethoxy-butyl]-amine
Synonyms: Dibenzyl-[(1S,2R)-1-(tert-butyl-dimethyl-silanyloxymethyl)-4-[1,3]dioxolan-2-yl-2-methoxymethoxy-butyl]-amine
CAS NO:305838-46-4
Molecular Formula:
Molecular Weight: 529.792
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: Dibenzyl-[(1S,2R)-1-(tert-butyl-dimethyl-silanyloxymethyl)-4-[1,3]dioxolan-2-yl-2-methoxymethoxy-butyl]-amine(CAS DataBase Reference)
NIST Chemistry Reference: Dibenzyl-[(1S,2R)-1-(tert-butyl-dimethyl-silanyloxymethyl)-4-[1,3]dioxolan-2-yl-2-methoxymethoxy-butyl]-amine(305838-46-4)
EPA Substance Registry System: Dibenzyl-[(1S,2R)-1-(tert-butyl-dimethyl-silanyloxymethyl)-4-[1,3]dioxolan-2-yl-2-methoxymethoxy-butyl]-amine(305838-46-4)

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: 305838-46-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 305838-46-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,5,8,3 and 8 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 305838-46:
(8*3)+(7*0)+(6*5)+(5*8)+(4*3)+(3*8)+(2*4)+(1*6)=144
144 % 10 = 4
So 305838-46-4 is a valid CAS Registry Number.

305838-46-4Upstream product

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305838-46-4Relevant academic research and scientific papers

An efficient stereoselective and stereodivergent synthesis of (2R,3R)- and (2R,3S)-3-hydroxypipecolic acids

Jourdant,Zhu

, p. 7033 - 7036 (2000)

Asymmetric syntheses of (2R,3R) and (2R,3S)-3-hydroxypipecolic acids are reported featuring a key diastereoselective addition of Buchi's Grignard reagent to the chiral serinal L-5. Based on conformational analysis, a stereocontrolled reduction of piperidi

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