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800401-64-3

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800401-64-3 Usage

General Description

1H-Pyrrolo[3,2-c]pyridine-2-carboxylic acid ethyl ester is a chemical compound with the molecular formula C11H10N2O2. It is an ethyl ester derivative of pyrrolo[3,2-c]pyridine-2-carboxylic acid, which is a heterocyclic compound with potential biological activity. This chemical may have applications in pharmaceutical research and drug development due to its structural similarity to other bioactive compounds. It is important to handle and use this chemical with care, following proper safety protocols and regulations.

Check Digit Verification of cas no

The CAS Registry Mumber 800401-64-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,0,0,4,0 and 1 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 800401-64:
(8*8)+(7*0)+(6*0)+(5*4)+(4*0)+(3*1)+(2*6)+(1*4)=103
103 % 10 = 3
So 800401-64-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H10N2O2/c1-2-14-10(13)9-5-7-6-11-4-3-8(7)12-9/h3-6,12H,2H2,1H3

800401-64-3SDS

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 Ethyl 1H-pyrrolo[3,2-c]pyridine-2-carboxylate

1.2 Other means of identification

Product number -
Other names ethyl 1H-pyrrolo[3,2-c]pyridine-2-carboxylate

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:800401-64-3 SDS

800401-64-3Relevant articles and documents

Asymmetric Hydrogenation of Azaindoles: Chemo- and Enantioselective Reduction of Fused Aromatic Ring Systems Consisting of Two Heteroarenes

Makida, Yusuke,Saita, Masahiro,Kuramoto, Takahiro,Ishizuka, Kentaro,Kuwano, Ryoichi

, p. 11859 - 11862 (2016/11/16)

High enantioselectivity was achieved for the hydrogenation of azaindoles by using the chiral catalyst, which was prepared from [Ru(η3-methallyl)2(cod)] and a trans-chelating bis(phosphine) ligand (PhTRAP). The dearomative reaction exclusively occurred on the five-membered ring, thus giving the corresponding azaindolines with up to 97:3 enantiomer ratio.

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