Basic information

Product Name: 1H-Indole-3-propanoic acid, b-oxo-1-(phenylmethyl)-, methyl ester
Synonyms:
CAS NO:61364-30-5
Molecular Formula: C19H17NO3
Molecular Weight: 307.349
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: 1H-Indole-3-propanoic acid, b-oxo-1-(phenylmethyl)-, methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 1H-Indole-3-propanoic acid, b-oxo-1-(phenylmethyl)-, methyl ester(61364-30-5)
EPA Substance Registry System: 1H-Indole-3-propanoic acid, b-oxo-1-(phenylmethyl)-, methyl ester(61364-30-5)

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: 61364-30-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 61364-30-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,3,6 and 4 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 61364-30:
(7*6)+(6*1)+(5*3)+(4*6)+(3*4)+(2*3)+(1*0)=105
105 % 10 = 5
So 61364-30-5 is a valid CAS Registry Number.

61364-30-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name	3-(1-benzyl-indol-3-yl)-3-oxo-propionic acid methyl ester

1.2 Other means of identification

Product number	-
Other names	3-(1-Benzyl-1H-indol-3-yl)-3-oxo-propionic acid methyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses	For industry use only.
Uses advised against	no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number	-
Service hours	Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

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61364-30-5Relevant academic research and scientific papers

Synthesis of tetrahydroindolones and tetrahydrocarbazolones via palladium catalyzed C–H activation

Zhang, Tiantian,Xu, Hongjin,Song, Chuanjun,Chang, Junbiao

, p. 4562 - 4565 (2018/11/23)

The treatment of bromo homoallyl pyrrolyl/indolyl ketone derivatives with Pd(OAc)2 in the presence of PPh3 and Cs2CO3 in DMF resulted in the formation of tetrahydroindolones and tetrahydrocarbazolones in moderate to good isolated yields.

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