Cas 114885-95-9,(S)-(-)-1-<(5-metoxy-1,4-cyclohexadienyl)methyl>-1,2,3,4-tetrahydro-β-carboline

114885-95-9

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Basic information

Product Name: (S)-(-)-1-<(5-metoxy-1,4-cyclohexadienyl)methyl>-1,2,3,4-tetrahydro-β-carboline
Synonyms: (S)-(-)-1-<(5-metoxy-1,4-cyclohexadienyl)methyl>-1,2,3,4-tetrahydro-β-carboline
CAS NO:114885-95-9
Molecular Formula:
Molecular Weight: 280.37
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: (S)-(-)-1-<(5-metoxy-1,4-cyclohexadienyl)methyl>-1,2,3,4-tetrahydro-β-carboline(CAS DataBase Reference)
NIST Chemistry Reference: (S)-(-)-1-<(5-metoxy-1,4-cyclohexadienyl)methyl>-1,2,3,4-tetrahydro-β-carboline(114885-95-9)
EPA Substance Registry System: (S)-(-)-1-<(5-metoxy-1,4-cyclohexadienyl)methyl>-1,2,3,4-tetrahydro-β-carboline(114885-95-9)

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: 114885-95-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 114885-95-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,8,8 and 5 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 114885-95:
(8*1)+(7*1)+(6*4)+(5*8)+(4*8)+(3*5)+(2*9)+(1*5)=149
149 % 10 = 9
So 114885-95-9 is a valid CAS Registry Number.

114885-95-9Upstream product

114926-72-6 (S)-(-)-1-<(5-metoxy-1,4-cyclohexadienyl)methyl>-1,2,3,4-tetrahydro-β-carboline

114885-95-9Downstream Products

114885-95-9Relevant academic research and scientific papers

Chiral and Achiral Formamidines in Synthesis. The First Asymmetric Route to (-)-Yohimbone and an Efficient Total Synthesis of (+/-)-Yohimbone

Meyers, A. I.,Miller, Donald B.,White, Franklin H.

, p. 4778 - 4787 (2007/10/02)

An asymmetric synthesis of (-)-yohimbone from chiral formamidines is presented.The synthetic pathway intercepts a previously reported route to yohimbenone (6) reported by Winterfeldt.An investigation of the -rearrangement involving iminium salts 8 an

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