Cas 609355-96-6,Benzyl-[2-((3aR,5R,6S,6aR)-6-benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-ethyl]-amine

609355-96-6

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Basic information

Product Name: Benzyl-[2-((3aR,5R,6S,6aR)-6-benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-ethyl]-amine
Synonyms: Benzyl-[2-((3aR,5R,6S,6aR)-6-benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-ethyl]-amine
CAS NO:609355-96-6
Molecular Formula:
Molecular Weight: 383.488
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: Benzyl-[2-((3aR,5R,6S,6aR)-6-benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-ethyl]-amine(CAS DataBase Reference)
NIST Chemistry Reference: Benzyl-[2-((3aR,5R,6S,6aR)-6-benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-ethyl]-amine(609355-96-6)
EPA Substance Registry System: Benzyl-[2-((3aR,5R,6S,6aR)-6-benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-ethyl]-amine(609355-96-6)

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: 609355-96-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 609355-96-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,9,3,5 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 609355-96:
(8*6)+(7*0)+(6*9)+(5*3)+(4*5)+(3*5)+(2*9)+(1*6)=176
176 % 10 = 6
So 609355-96-6 is a valid CAS Registry Number.

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609355-96-6Relevant academic research and scientific papers

An expeditious synthesis of a (3S,4S,5R)-trihydroxyazepane

Dhavale, Dilip D.,Chaudhari, Vinod D.,Tilekar, Jayant N.

, p. 7321 - 7323 (2003)

A practical approach for the synthesis of the (2S,3S,4R)-trihydroxyazepane 1d has been reported. Starting from α-D-xylo-pentodialdose, readily available from D-glucose, the sequence involves Wittig olefination and reductive amination as key steps.

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