Cas 888323-28-2,(3R,4R,5R,6R)-4-Benzyloxy-6-benzyloxymethyl-5-butoxy-1-butyl-piperidin-3-ol

888323-28-2

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Basic information

Product Name: (3R,4R,5R,6R)-4-Benzyloxy-6-benzyloxymethyl-5-butoxy-1-butyl-piperidin-3-ol
Synonyms:
CAS NO:888323-28-2
Molecular Formula:
Molecular Weight: 455.638
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: (3R,4R,5R,6R)-4-Benzyloxy-6-benzyloxymethyl-5-butoxy-1-butyl-piperidin-3-ol(CAS DataBase Reference)
NIST Chemistry Reference: (3R,4R,5R,6R)-4-Benzyloxy-6-benzyloxymethyl-5-butoxy-1-butyl-piperidin-3-ol(888323-28-2)
EPA Substance Registry System: (3R,4R,5R,6R)-4-Benzyloxy-6-benzyloxymethyl-5-butoxy-1-butyl-piperidin-3-ol(888323-28-2)

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: 888323-28-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 888323-28-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,8,3,2 and 3 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 888323-28:
(8*8)+(7*8)+(6*8)+(5*3)+(4*2)+(3*3)+(2*2)+(1*8)=212
212 % 10 = 2
So 888323-28-2 is a valid CAS Registry Number.

888323-28-2Upstream product

858675-45-3 3,6-di-O-benzyl-N-butyl-4-O-butyl-1,5-dideoxy-1,5-imino-D-glucitol

888323-28-2Downstream Products

888323-28-2Relevant academic research and scientific papers

A stereodivergent approach to 1-deoxynojirimycin, 1-deoxygalactonojirimycin and 1-deoxymannojirimycin derivatives

Boucheron, Charlotte,Compain, Philippe,Martin, Olivier R.

, p. 3081 - 3084 (2007/10/03)

A stereodivergent synthesis of N-alkylated 1-deoxygalactonojirimycin and 1-deoxymannojirimycin derivatives has been achieved from a protected 1-deoxynojirimycin intermediate having two free OH groups tactically positioned at C-2 and C-4. The inversion of

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