Cas 1374005-03-4,(5-benzyloxy-4-[2-(4-benzyloxy-3-methoxy-phenyl)-acetyl]-1H-indol-3-yl)-oxo-acetic acid methyl ester

1374005-03-4

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Basic information

Product Name: (5-benzyloxy-4-[2-(4-benzyloxy-3-methoxy-phenyl)-acetyl]-1H-indol-3-yl)-oxo-acetic acid methyl ester
Synonyms: (5-benzyloxy-4-[2-(4-benzyloxy-3-methoxy-phenyl)-acetyl]-1H-indol-3-yl)-oxo-acetic acid methyl ester
CAS NO:1374005-03-4
Molecular Formula:
Molecular Weight: 563.607
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: (5-benzyloxy-4-[2-(4-benzyloxy-3-methoxy-phenyl)-acetyl]-1H-indol-3-yl)-oxo-acetic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (5-benzyloxy-4-[2-(4-benzyloxy-3-methoxy-phenyl)-acetyl]-1H-indol-3-yl)-oxo-acetic acid methyl ester(1374005-03-4)
EPA Substance Registry System: (5-benzyloxy-4-[2-(4-benzyloxy-3-methoxy-phenyl)-acetyl]-1H-indol-3-yl)-oxo-acetic acid methyl ester(1374005-03-4)

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: 1374005-03-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1374005-03-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,4,0,0 and 5 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1374005-03:
(9*1)+(8*3)+(7*7)+(6*4)+(5*0)+(4*0)+(3*5)+(2*0)+(1*3)=124
124 % 10 = 4
So 1374005-03-4 is a valid CAS Registry Number.

1374005-03-4Upstream product

67-56-1 methanol

1374005-03-4Downstream Products

1374005-04-5 6-benzyloxy-4-(4-benzyloxy-3-methoxy-phenyl)-5-oxo-1,5-dihydro-benzo[cd]indole-3-carboxylic acid methyl ester

1374005-03-4Relevant academic research and scientific papers

Synthetic studies of decursivine derivatives: Preparation of key indole alkaloids via α-hydroxyalkylation

Ito, Fumihiro,Yamaguchi, Kentaro

experimental part, p. 3708 - 3716 (2012/06/30)

2-Hydroxyacetyl indole modified at C-3 position was prepared with an eye to developing a total synthesis of decursivine derivatives (decursivine, serotobenine, moschaminindolol, and flavumindole). The indole was prepared through a sequence of oxalyl chlor

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