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5-(Benzyloxy)-4-(methoxymethyl)-9H-pyrido[3,4-b]indole-3-carboxylic acid ethyl ester is a complex organic compound with the molecular formula C22H21NO5. It is a derivative of the pyridoindole class of compounds, which are known for their diverse biological activities. This specific compound features a pyridoindole core, with a benzyloxy group at the 5-position, a methoxymethyl group at the 4-position, and an ethyl ester group attached to the carboxylic acid at the 3-position. The compound is synthesized for potential applications in pharmaceutical research, particularly in the development of new drugs targeting various diseases. Its structure allows for further chemical modifications, making it a valuable intermediate in the synthesis of more complex molecules with potential therapeutic properties.

83910-34-3

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83910-34-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83910-34-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,9,1 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 83910-34:
(7*8)+(6*3)+(5*9)+(4*1)+(3*0)+(2*3)+(1*4)=133
133 % 10 = 3
So 83910-34-3 is a valid CAS Registry Number.

83910-34-3SDS

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 9H-Pyrido[3,4-b]indole-3-carboxylic acid, 4-(methoxymethyl)-5-(phenylmethoxy)-, ethyl ester

1.2 Other means of identification

Product number -
Other names ZK 91296

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:83910-34-3 SDS

83910-34-3Downstream Products

83910-34-3Relevant academic research and scientific papers

Process for the production of β-carbolines by dehydrogenation

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, (2008/06/13)

β-carbolines of formula I STR1 wherein R=C1-5 alkyl R4 =H, C1-5 alkyl or --(CH2)n --OR with n=1 or 2 and RA =H, R, (CHR)n --OR, OCH2 Ph, OPh, OPh(Cl,Br),OR,OCH2/

Pharmacologically active 3-substituted beta-carbolines useful as tranquilizers

-

, (2008/06/13)

3-Substituted beta-carbolines of the formula STR1 wherein RA is H, F, Cl, Br, I, NO2, CN, CH3, CF3, SCH3, NR16 R17 or NHCOR16, wherein R16 and R17/sup

Pharmacologically active 3-substituted beta-carbolines

-

, (2008/06/13)

3-substituted beta-carbolines of the formula STR1 wherein R C is hydrogen, lower alkyl, alkoxyalkyl of up to 6 C-atoms, cycloalkyl of 3-6 C-atoms, aralkyl of up to 8 C-atoms, or (CH 2) n OR 20wherein R 20 is alkyl of up to 6 C-atoms, cycloalkyl of 3-6 C-a

SYNTHESIS OF 4-SUBSTITUTED β-CARBOLINES

Neef, Guenter,Eder, Ulrich,Huth, Andreas,Rahtz, Dieter,Schmiechen, Ralph,Seidelmann, Dieter

, p. 1295 - 1313 (2007/10/02)

Various 4-substituted β-carbolines are synthesized and further modified by electrophilic substitution reactions.The regioselectivity of electrophilic attack is demonstrated for a number of different reactions and strategies are outlined to achieve substit

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