Basic information

Product Name: 1H-Indole, 3-(5-pentyl-2-thienyl)-1-(phenylmethyl)-
Synonyms:
CAS NO:89036-29-3
Molecular Formula: C24H25NS
Molecular Weight: 359.535
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-(5-pentyl-2-thienyl)-1-(phenylmethyl)-(CAS DataBase Reference)
NIST Chemistry Reference: 1H-Indole, 3-(5-pentyl-2-thienyl)-1-(phenylmethyl)-(89036-29-3)
EPA Substance Registry System: 1H-Indole, 3-(5-pentyl-2-thienyl)-1-(phenylmethyl)-(89036-29-3)

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: 89036-29-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 89036-29-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,0,3 and 6 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 89036-29:
(7*8)+(6*9)+(5*0)+(4*3)+(3*6)+(2*2)+(1*9)=153
153 % 10 = 3
So 89036-29-3 is a valid CAS Registry Number.

89036-29-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name	1-benzyl-3-(5-pentylthiophen-2-yl)indole

1.2 Other means of identification

Product number	-
Other names	1H-Indole,3-(5-pentyl-2-thienyl)-1-(phenylmethyl)

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:89036-29-3 SDS

89036-29-3Upstream product

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89036-29-3Relevant academic research and scientific papers

2. BORON TRIFLURIDE ACTIVATED 3-THIAZOLINES. A VERSATILE SYNTHESIS OF THIOPHENES

Meltz, Clifford N.,Volkmann, Robert A.

, p. 4507 - 4510 (2007/10/02)

Thiazolidines generated by the addition of ketone enolates to boron trifluoride activated 2,2,5-trialkyl-3-thiazolines undergo a facile acid catalyzed conversion to di- and trisubstituted thiophenes.

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