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[6aS,(-)]-8α-Chloro-9β-ethenyl-2,6,6aβ,7,8,9-hexahydro-10-isocyano-6,6,9-trimethylnaphtho[1,2,3-cd]indole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

101968-76-7

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101968-76-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 101968-76-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,9,6 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 101968-76:
(8*1)+(7*0)+(6*1)+(5*9)+(4*6)+(3*8)+(2*7)+(1*6)=127
127 % 10 = 7
So 101968-76-7 is a valid CAS Registry Number.

101968-76-7SDS

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 hapalindole I

1.2 Other means of identification

Product number -
Other names -

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:101968-76-7 SDS

101968-76-7Upstream product

101968-76-7Downstream Products

101968-76-7Relevant academic research and scientific papers

Fontonamide and Anhydrohapaloxindole A, Two New Alkaloids from the Blue-Green Alga Hapalosiphon fontinalis

Moore, Richard E.,Yang, Xu-Qiang G.,Patterson, Gregory M. L.

, p. 3773 - 3777 (2007/10/02)

Fontonamide (3) and anhydrohapaloxindole A (4) are two minor alkaloids that have been isolated from a cultured strain of the terrestrial blue-green alga Hapalosiphon fontinalis.Both compounds appear to be singlet oxygen oxidation products of hapalindole A (1), the major alkaloid in this cyanophyte.Hapalonamide A (5), the probable precursor of fontonamide, is formed along with 3 and 4 when an oxygen-aerated solution of 1 in aqueous methanol buffered at pH 8 with sodium phosphate and containing a trace of rose bengal is irradiated at room temperature.To date, however, 5 has not been identified as a constituent of H. fontinalis.

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