Cas 330799-51-4,(1S,2S,5R,6R)-3-aza-3-benzyl-6-(N-(9-fluorenylmethoxycarbonyl)aminomethyl)bicyclo[3.1.0]hexyl-2-methanol

330799-51-4

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Basic information

Product Name: (1S,2S,5R,6R)-3-aza-3-benzyl-6-(N-(9-fluorenylmethoxycarbonyl)aminomethyl)bicyclo[3.1.0]hexyl-2-methanol
Synonyms: (1S,2S,5R,6R)-3-aza-3-benzyl-6-(N-(9-fluorenylmethoxycarbonyl)aminomethyl)bicyclo[3.1.0]hexyl-2-methanol
CAS NO:330799-51-4
Molecular Formula:
Molecular Weight: 454.569
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,2S,5R,6R)-3-aza-3-benzyl-6-(N-(9-fluorenylmethoxycarbonyl)aminomethyl)bicyclo[3.1.0]hexyl-2-methanol(CAS DataBase Reference)
NIST Chemistry Reference: (1S,2S,5R,6R)-3-aza-3-benzyl-6-(N-(9-fluorenylmethoxycarbonyl)aminomethyl)bicyclo[3.1.0]hexyl-2-methanol(330799-51-4)
EPA Substance Registry System: (1S,2S,5R,6R)-3-aza-3-benzyl-6-(N-(9-fluorenylmethoxycarbonyl)aminomethyl)bicyclo[3.1.0]hexyl-2-methanol(330799-51-4)

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: 330799-51-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 330799-51-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,0,7,9 and 9 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 330799-51:
(8*3)+(7*3)+(6*0)+(5*7)+(4*9)+(3*9)+(2*5)+(1*1)=154
154 % 10 = 4
So 330799-51-4 is a valid CAS Registry Number.

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330799-51-4Relevant academic research and scientific papers

Solid-phase guanidinylation as a diversification strategy of poly-L-proline type II peptide mimic scaffolds.

Mamai,Madalengoitia

, p. 561 - 564 (2001)

[reaction: see text] Solid-phase guanidinylation of proline-templated amino acids is studied as a diversification strategy of poly-L-proline type II scaffolds.

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