Cas 331447-75-7,2-[2-benzyloxycarbonylamino-3-(1H-indol-3-yl)-propionylamino]-6-tert-butoxycarbonylamino-hexanoic acid tert-butyl ester

331447-75-7

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Basic information

Product Name: 2-[2-benzyloxycarbonylamino-3-(1H-indol-3-yl)-propionylamino]-6-tert-butoxycarbonylamino-hexanoic acid tert-butyl ester
Synonyms:
CAS NO:331447-75-7
Molecular Formula:
Molecular Weight: 622.762
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: 2-[2-benzyloxycarbonylamino-3-(1H-indol-3-yl)-propionylamino]-6-tert-butoxycarbonylamino-hexanoic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-[2-benzyloxycarbonylamino-3-(1H-indol-3-yl)-propionylamino]-6-tert-butoxycarbonylamino-hexanoic acid tert-butyl ester(331447-75-7)
EPA Substance Registry System: 2-[2-benzyloxycarbonylamino-3-(1H-indol-3-yl)-propionylamino]-6-tert-butoxycarbonylamino-hexanoic acid tert-butyl ester(331447-75-7)

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: 331447-75-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 331447-75-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,1,4,4 and 7 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 331447-75:
(8*3)+(7*3)+(6*1)+(5*4)+(4*4)+(3*7)+(2*7)+(1*5)=127
127 % 10 = 7
So 331447-75-7 is a valid CAS Registry Number.

331447-75-7Upstream product

331447-75-7Downstream Products

331447-75-7Relevant academic research and scientific papers

Small molecule somatostatin receptor subtype-2 antagonists

Hay, Bruce A.,Cole, Bridget M.,DiCapua, Frank,Kirk, Glen W.,Murray, Marianne C.,Nardone, Rona A.,Pelletier, Dennis J.,Ricketts, Anthony P.,Robertson, Alan S.,Siegel, Todd W.

, p. 2731 - 2734 (2001)

The first potent small molecule sst2 antagonists are reported. Altering known sst2 agonist molecules yielded compounds with high sst2 binding affinity and full antagonist activity. Compound 7a, for example, displaced somatostatin binding to the sst2 recep

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