Cas 398460-13-4,(-)-(1S,4S,5S)-N-benzyloxy-4-hydroxy-1-O-(2,2,2-trichloroethyl)-2,3-dideoxyhex-2-enopyranuronamide

398460-13-4

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Basic information

Product Name: (-)-(1S,4S,5S)-N-benzyloxy-4-hydroxy-1-O-(2,2,2-trichloroethyl)-2,3-dideoxyhex-2-enopyranuronamide
Synonyms: (-)-(1S,4S,5S)-N-benzyloxy-4-hydroxy-1-O-(2,2,2-trichloroethyl)-2,3-dideoxyhex-2-enopyranuronamide
CAS NO:398460-13-4
Molecular Formula:
Molecular Weight: 396.655
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: (-)-(1S,4S,5S)-N-benzyloxy-4-hydroxy-1-O-(2,2,2-trichloroethyl)-2,3-dideoxyhex-2-enopyranuronamide(CAS DataBase Reference)
NIST Chemistry Reference: (-)-(1S,4S,5S)-N-benzyloxy-4-hydroxy-1-O-(2,2,2-trichloroethyl)-2,3-dideoxyhex-2-enopyranuronamide(398460-13-4)
EPA Substance Registry System: (-)-(1S,4S,5S)-N-benzyloxy-4-hydroxy-1-O-(2,2,2-trichloroethyl)-2,3-dideoxyhex-2-enopyranuronamide(398460-13-4)

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: 398460-13-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 398460-13-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,9,8,4,6 and 0 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 398460-13:
(8*3)+(7*9)+(6*8)+(5*4)+(4*6)+(3*0)+(2*1)+(1*3)=184
184 % 10 = 4
So 398460-13-4 is a valid CAS Registry Number.

398460-13-4Upstream product

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398460-13-4Relevant academic research and scientific papers

Conversion of glucuronic acid glycosides to novel bicyclic β-lactams

Durham, Timothy B.,Miller, Marvin J.

, p. 135 - 138 (2007/10/03)

(matrix presented) Methodology for the conversion of glucuronic acid glycosides to novel bicyclic β-lactams is reported. Using this strategy, we prepared two novel templates suitable for use in combinatorial chemistry strategies for the construction of a

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