Cas 320589-60-4,methyl (1R,3S)-1-cyclohexyl-1,2,3,4-tetrahydro-2-N'-tert-butoxycarbonylglycinyl-β-carboline-3-carboxylate

320589-60-4

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Basic information

Product Name: methyl (1R,3S)-1-cyclohexyl-1,2,3,4-tetrahydro-2-N'-tert-butoxycarbonylglycinyl-β-carboline-3-carboxylate
Synonyms: methyl (1R,3S)-1-cyclohexyl-1,2,3,4-tetrahydro-2-N'-tert-butoxycarbonylglycinyl-β-carboline-3-carboxylate
CAS NO:320589-60-4
Molecular Formula:
Molecular Weight: 469.581
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: methyl (1R,3S)-1-cyclohexyl-1,2,3,4-tetrahydro-2-N'-tert-butoxycarbonylglycinyl-β-carboline-3-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: methyl (1R,3S)-1-cyclohexyl-1,2,3,4-tetrahydro-2-N'-tert-butoxycarbonylglycinyl-β-carboline-3-carboxylate(320589-60-4)
EPA Substance Registry System: methyl (1R,3S)-1-cyclohexyl-1,2,3,4-tetrahydro-2-N'-tert-butoxycarbonylglycinyl-β-carboline-3-carboxylate(320589-60-4)

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: 320589-60-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 320589-60-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,0,5,8 and 9 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 320589-60:
(8*3)+(7*2)+(6*0)+(5*5)+(4*8)+(3*9)+(2*6)+(1*0)=134
134 % 10 = 4
So 320589-60-4 is a valid CAS Registry Number.

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320589-60-4Relevant academic research and scientific papers

The fate of the tryptophan stereocenter in the synthesis of 7,10,16,16a-tetrahydro-11H-quinazolino[2',3':3,4]pyrazino[1,2-b]β-carboline-5,8-diones

Madrigal, Antonio,Grande, Mercedes,Avendao, Carmen

, p. 3515 - 3526 (2000)

Condensation reactions of anthranilic acid with iminoethers 14-17 derived from tetracycles 9-13 to give the title hexacyclic compounds reflect a preferred trans-relationship for H(10)-H(16a) protons in C(7)-unsubstituted products and a cis-relatioship for

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