Cas 155688-54-3,1,4,6-trideoxy-1,4-(tert-butoxycarbonyl)imino-2,3-O-isopropylidene-6-((phenylmethyl)amino)-D-mannitol

155688-54-3

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Basic information

Product Name: 1,4,6-trideoxy-1,4-(tert-butoxycarbonyl)imino-2,3-O-isopropylidene-6-((phenylmethyl)amino)-D-mannitol
Synonyms: 1,4,6-trideoxy-1,4-(tert-butoxycarbonyl)imino-2,3-O-isopropylidene-6-((phenylmethyl)amino)-D-mannitol
CAS NO:155688-54-3
Molecular Formula:
Molecular Weight: 392.495
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: 1,4,6-trideoxy-1,4-(tert-butoxycarbonyl)imino-2,3-O-isopropylidene-6-((phenylmethyl)amino)-D-mannitol(CAS DataBase Reference)
NIST Chemistry Reference: 1,4,6-trideoxy-1,4-(tert-butoxycarbonyl)imino-2,3-O-isopropylidene-6-((phenylmethyl)amino)-D-mannitol(155688-54-3)
EPA Substance Registry System: 1,4,6-trideoxy-1,4-(tert-butoxycarbonyl)imino-2,3-O-isopropylidene-6-((phenylmethyl)amino)-D-mannitol(155688-54-3)

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: 155688-54-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 155688-54-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,6,8 and 8 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 155688-54:
(8*1)+(7*5)+(6*5)+(5*6)+(4*8)+(3*8)+(2*5)+(1*4)=173
173 % 10 = 3
So 155688-54-3 is a valid CAS Registry Number.

155688-54-3Upstream product

155688-54-3Downstream Products

155688-54-3Relevant academic research and scientific papers

Pyrrolidine and Hexahydro-1H-Azepine Mimics of the "Flap Up" Mannosyl Cation

Farr, Robert A.,Holland, Amy K.,Huber, Edward W.,Peet, Norton P.,Weintraub, Philip M.

, p. 1033 - 1044 (2007/10/02)

The pyrrolidine 4, 6-amino-1,4,6-trideoxy-1,4-imino-D-mannitol dihydrochloride, and the hexahydro-1H-azepine 5, 4-amino-1,4,6-trideoxy-1,6-imino-D-mannitol dihydrochloride, were synthesized as potential inhibitors of α-mannosidase.

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