Cas 884871-60-7,1-benzyloxymethyl-2-bromo-5-(2,2-dimethyl[1,3]dioxolan-4-ylmethyl)-4-(1,1-dimethylprop-2-ynyl)-1H-imidazole

884871-60-7

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Basic information

Product Name: 1-benzyloxymethyl-2-bromo-5-(2,2-dimethyl[1,3]dioxolan-4-ylmethyl)-4-(1,1-dimethylprop-2-ynyl)-1H-imidazole
Synonyms: 1-benzyloxymethyl-2-bromo-5-(2,2-dimethyl[1,3]dioxolan-4-ylmethyl)-4-(1,1-dimethylprop-2-ynyl)-1H-imidazole
CAS NO:884871-60-7
Molecular Formula:
Molecular Weight: 447.372
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-benzyloxymethyl-2-bromo-5-(2,2-dimethyl[1,3]dioxolan-4-ylmethyl)-4-(1,1-dimethylprop-2-ynyl)-1H-imidazole(CAS DataBase Reference)
NIST Chemistry Reference: 1-benzyloxymethyl-2-bromo-5-(2,2-dimethyl[1,3]dioxolan-4-ylmethyl)-4-(1,1-dimethylprop-2-ynyl)-1H-imidazole(884871-60-7)
EPA Substance Registry System: 1-benzyloxymethyl-2-bromo-5-(2,2-dimethyl[1,3]dioxolan-4-ylmethyl)-4-(1,1-dimethylprop-2-ynyl)-1H-imidazole(884871-60-7)

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: 884871-60-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 884871-60-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,4,8,7 and 1 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 884871-60:
(8*8)+(7*8)+(6*4)+(5*8)+(4*7)+(3*1)+(2*6)+(1*0)=227
227 % 10 = 7
So 884871-60-7 is a valid CAS Registry Number.

884871-60-7Upstream product

884871-60-7Downstream Products

884871-60-7Relevant academic research and scientific papers

Explorations on the total synthesis of the unusual marine alkaloid chartelline A

Sun, Cuixiang,Lin, Xichen,Weinreb, Steven M.

, p. 3159 - 3166 (2006)

In work directed toward a total synthesis of chartelline A (1a), a strategy was investigated to construct the 10-membered ring of this marine alkaloid via an intramolecular aldehyde/β-lactam cyclocondensation to form the macrocyclic enamide functionality.

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