Basic information

Product Name: 1H-Indole-3-propanoic acid, 4-nitrophenyl ester
Synonyms:
CAS NO:35665-88-4
Molecular Formula: C17H14N2O4
Molecular Weight: 310.309
EINECS: N/A
Product Categories: N/A
Mol File: 35665-88-4.mol

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, 4-nitrophenyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 1H-Indole-3-propanoic acid, 4-nitrophenyl ester(35665-88-4)
EPA Substance Registry System: 1H-Indole-3-propanoic acid, 4-nitrophenyl ester(35665-88-4)

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: 35665-88-4(Hazardous Substances Data)

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35665-88-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35665-88-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,6,6 and 5 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 35665-88:
(7*3)+(6*5)+(5*6)+(4*6)+(3*5)+(2*8)+(1*8)=144
144 % 10 = 4
So 35665-88-4 is a valid CAS Registry Number.

35665-88-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name	4-Nitrophenyl 3-(1H-Indol-3-yl)propanoate

1.2 Other means of identification

Product number	-
Other names	p-nitrophenyl 3-indolepropionate

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).

More Details:35665-88-4 SDS

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35665-88-4Relevant academic research and scientific papers

Synthetic Analogues of Naturally Occurring Spider Toxins

Kovacs, Lajos,Hesse, Manfred

, p. 1909 - 1924 (1992)

Naturally occurring spider toxins are potent inhibitors of glutamate receptors of the central nervous system and have the general structure (hetero)arylacyl->aminoacyl(I)-polyamine-aminoacyl(II) (the arrow indicates the direction of an amide linkage).In

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