Welcome to LookChem.com Sign In|Join Free
  • or
4-Methoxy-1-methoxycarbonyl-beta-carboline is a complex nitrogen-containing heterocyclic chemical compound that belongs to the beta-carboline family. It is characterized by the presence of a methoxy functional group, which is a methyl group linked to an oxygen atom, and a methoxycarbonyl functional group, which is a combination of the methoxy and carbonyl functional groups. Despite its unique structure, the specific properties, uses, and potential health impacts of this carboline are not extensively documented or studied, possibly due to its specialized applications in chemical research.

60807-25-2

Post Buying Request

60807-25-2 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

60807-25-2 Usage

Uses

Given the limited information on the uses of 4-Methoxy-1-methoxycarbonyl-beta-carboline, the following applications are inferred based on its chemical structure and the general applications of beta-carboline compounds:
Used in Chemical Research:
4-Methoxy-1-methoxycarbonyl-beta-carboline is used as a research compound for studying the properties and behavior of beta-carboline derivatives. Its unique structure allows scientists to explore its potential interactions with other molecules and its role in various chemical reactions.
Used in Pharmaceutical Development:
Although not well-documented, 4-Methoxy-1-methoxycarbonyl-beta-carboline may be used as a starting material or intermediate in the synthesis of pharmaceutical compounds. Its methoxy and methoxycarbonyl functional groups could potentially be modified to create new drug candidates with specific therapeutic properties.
Used in Material Science:
The unique structure of 4-Methoxy-1-methoxycarbonyl-beta-carboline may also find applications in material science, where its properties could be harnessed to develop new materials with specific characteristics, such as improved stability, conductivity, or reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 60807-25-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,8,0 and 7 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 60807-25:
(7*6)+(6*0)+(5*8)+(4*0)+(3*7)+(2*2)+(1*5)=112
112 % 10 = 2
So 60807-25-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H12N2O3/c1-18-10-7-15-13(14(17)19-2)12-11(10)8-5-3-4-6-9(8)16-12/h3-7,16H,1-2H3

60807-25-2SDS

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 methyl 4-methoxy-9H-pyrido[3,4-b]indole-1-carboxylate

1.2 Other means of identification

Product number -
Other names W1176

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:60807-25-2 SDS

60807-25-2Relevant academic research and scientific papers

A general synthetic route for 1-substituted 4-oxygenated β-carbolines (synthetic studies on indoles and related compounds 41)

Suzuki, Hideharu,Iwata, Chiemi,Sakurai, Katsumi,Tokumoto, Kazuhiko,Takahashi, Hiroko,Hanada, Masako,Yokoyama, Yuusaku,Murakami, Yasuoki

, p. 1593 - 1606 (2007/10/03)

A new synthetic route for two naturally occurring 1-substituted 4-methoxy-β-carbolines (1b, c) is described. This synthetic route involves elaboration of the ester groups in ethyl indole-2-carboxylate (4b) and its 1-benzyl derivative (4a), C3-s

A new general synthetic route for 1-substituted 4-oxygenated β-carbolines

Suzuki,Yokoyama,Miyagi,Murakami

, p. 2170 - 2172 (2007/10/02)

Two natural]y occurring 1-substituted 4-methoxy-β-carboline (1b,c) were synthesized from ethyl indole-2-carboxylate (5b) and its 1-benzyl derivative (5a), respectively. The synthesis routes involved elaboration of the ester group of 5a,b, cyclization of t

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 60807-25-2