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102828-03-5

2-(9H-beta-carbolin-1-yl)ethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

102828-03-5

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102828-03-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102828-03-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,8,2 and 8 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 102828-03:
(8*1)+(7*0)+(6*2)+(5*8)+(4*2)+(3*8)+(2*0)+(1*3)=95
95 % 10 = 5
So 102828-03-5 is a valid CAS Registry Number.

102828-03-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(9H-pyrido[3,4-b]indol-1-yl)ethanol

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:102828-03-5 SDS

102828-03-5Downstream Products

102828-03-5Relevant articles and documents

Remarkable photocytotoxicity of a novel triazole-linked cationic porphyrin-β-carboline conjugate

Kumar, Dalip,Mishra, Bhupendra A.,Chandra Shekar,Kumar, Anil,Akamatsu, Kanako,Kusaka, Eriko,Ito, Takeo

, p. 683 - 685 (2013)

Employing a click chemistry approach we have synthesized a novel triazole-linked cationic porphyrin-β-carboline conjugate which exhibited remarkable photocytotoxicity against the A549 cancer cell line (IC50 = 60 nM).

A total synthesis of Manzamine C and its geometrical isomer

Torisawa,Hashimoto,Nakagawa,Seki,Hara,Hino

, p. 8067 - 8078 (2007/10/02)

Manzamine C (1) has been synthesized from silyloxyacetylene (3) along the line: 4→5→8→18→1. The overall yield is 21%. The β-carboline segment (11) was obtained by the Bischler-Napieralski reaction of 14 followed by dehydrogenation. By the similar procedur

A total synthesis of manzamine C

Torisawa,Hashimoto,Nakagawa,Hino

, p. 6549 - 6550 (2007/10/02)

Manzamine C (1) was synthesized by the conjunction of 6-(Z)-azacycloundecene (9) and 1-substituted β-carboline derivatives (10 or 13).

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