Cas 155885-28-2,(2S,3S)-2-[(S)-((4S,5S)-5-Benzyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-hydroxy-methyl]-pyrrolidin-3-ol

155885-28-2

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Basic information

Product Name: (2S,3S)-2-[(S)-((4S,5S)-5-Benzyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-hydroxy-methyl]-pyrrolidin-3-ol
Synonyms: (2S,3S)-2-[(S)-((4S,5S)-5-Benzyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-hydroxy-methyl]-pyrrolidin-3-ol
CAS NO:155885-28-2
Molecular Formula:
Molecular Weight: 337.416
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: (2S,3S)-2-[(S)-((4S,5S)-5-Benzyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-hydroxy-methyl]-pyrrolidin-3-ol(CAS DataBase Reference)
NIST Chemistry Reference: (2S,3S)-2-[(S)-((4S,5S)-5-Benzyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-hydroxy-methyl]-pyrrolidin-3-ol(155885-28-2)
EPA Substance Registry System: (2S,3S)-2-[(S)-((4S,5S)-5-Benzyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-hydroxy-methyl]-pyrrolidin-3-ol(155885-28-2)

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: 155885-28-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 155885-28-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,8,8 and 5 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 155885-28:
(8*1)+(7*5)+(6*5)+(5*8)+(4*8)+(3*5)+(2*2)+(1*8)=172
172 % 10 = 2
So 155885-28-2 is a valid CAS Registry Number.

155885-28-2Upstream product

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155885-28-2Relevant academic research and scientific papers

Hydroxy-directed Ketone Reduction. Application to the Synthesis of (+)-8,8a-Diepicastanospermine

Thompson, Stephen H. J.,Subramanian, R. Sankara,Roberts, John K.,Hadley, Michael S.,Gallagher, Timothy

, p. 933 - 934 (2007/10/02)

Reduction of heterocyclic-derived aldol adducts 2 and 3 using NaBH(OAc)3 is stereoselective and proceeds via a hydroxy-directed mechanism to give 6 and 7, respectively, thereby complementing the stereoselectivity available with NaBH4; a synthesis of (+)-8

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