Cas 379668-89-0,(4R,6S)-2-[benzyloxycarbonylamino]-4-[(3,3)-dimethoxypropyl]-6-methyl-3,4,5,6-tetrahydropyrimidine

379668-89-0

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Basic information

Product Name: (4R,6S)-2-[benzyloxycarbonylamino]-4-[(3,3)-dimethoxypropyl]-6-methyl-3,4,5,6-tetrahydropyrimidine
Synonyms: (4R,6S)-2-[benzyloxycarbonylamino]-4-[(3,3)-dimethoxypropyl]-6-methyl-3,4,5,6-tetrahydropyrimidine
CAS NO:379668-89-0
Molecular Formula:
Molecular Weight: 349.43
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: (4R,6S)-2-[benzyloxycarbonylamino]-4-[(3,3)-dimethoxypropyl]-6-methyl-3,4,5,6-tetrahydropyrimidine(CAS DataBase Reference)
NIST Chemistry Reference: (4R,6S)-2-[benzyloxycarbonylamino]-4-[(3,3)-dimethoxypropyl]-6-methyl-3,4,5,6-tetrahydropyrimidine(379668-89-0)
EPA Substance Registry System: (4R,6S)-2-[benzyloxycarbonylamino]-4-[(3,3)-dimethoxypropyl]-6-methyl-3,4,5,6-tetrahydropyrimidine(379668-89-0)

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: 379668-89-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 379668-89-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,7,9,6,6 and 8 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 379668-89:
(8*3)+(7*7)+(6*9)+(5*6)+(4*6)+(3*8)+(2*8)+(1*9)=230
230 % 10 = 0
So 379668-89-0 is a valid CAS Registry Number.

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379668-89-0Relevant academic research and scientific papers

Evolution of a strategy for the synthesis of structurally complex batzelladine alkaloids. Enantioselective total synthesis of the proposed structure of batzelladine F and structural revision

Cohen, Frederick,Overman, Larry E.

, p. 2594 - 2603 (2007/10/03)

Stereoselective synthesis of octahydro-5,6,6a-triazaacenaphthalenes 29 and 34 having the anti-relationship of the angular hydrogens flanking the pyrrolidine nitrogen confirmed suspicions that the relative configuration of the left-hand tricyclic guanidine

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