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6094-43-5

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6094-43-5 Usage

Physical state

Colorless to light yellow liquid

Odor

Floral and woody

Uses

Fragrance and flavoring agent in perfumes, cosmetics, and consumer products; synthesis of pharmaceuticals; chemical intermediate

Potential properties

Antimicrobial, antioxidant

Industrial applications

Various applications due to potential antimicrobial and antioxidant properties

Medical potential

Treatment of cancer (inhibiting cancer cell growth)

Check Digit Verification of cas no

The CAS Registry Mumber 6094-43-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,9 and 4 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6094-43:
(6*6)+(5*0)+(4*9)+(3*4)+(2*4)+(1*3)=95
95 % 10 = 5
So 6094-43-5 is a valid CAS Registry Number.

6094-43-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(2,3,3a,4,5,6,7,7a-octahydro-1H-indol-2-yl)propan-1-ol

1.2 Other means of identification

Product number -
Other names 3-octahydroindol-2-yl-propan-1-ol

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:6094-43-5 SDS

6094-43-5Downstream Products

6094-43-5Relevant articles and documents

SATURATED NITROGEN-CONTAINING HETEROCYCLES. 11. THE SYNTHESIS AND STRUCTURAL STUDIES OF OCTAHYDROINDOLYLALKANOLS

Krivcen'ko, A. P.,Nikolaeva, T. G.,Espenbetov, A. A.,Struchkov, Yu. T.,Kharchenko, V. G.

, p. 52 - 56 (2007/10/02)

A catalytic synthesis was carried out for 3-(1-R-2-octahydroindolyl)alkanols using nickel promoted by ruthenium, Raney nickel, and Raney cobalt previously treated with acetic acid.An x-ray diffraction structural study of the acid tartrate of 3-(1-methyl-2

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