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175975-76-5

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175975-76-5 Usage

Chemical Class

Indole alkaloids

Derivative of

Neurotransmitter serotonin

Presence

Found in various plants and fungi

Pharmacological activities

Effects on the central nervous system

Analgesic properties

Potential for pain relief

Anti-inflammatory properties

May help reduce inflammation

Potential as an antipsychotic

May help treat psychiatric disorders

Potential as an antihypertensive

May help lower blood pressure

Ongoing research

Uncovering potential therapeutic uses and biological activities

Check Digit Verification of cas no

The CAS Registry Mumber 175975-76-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,9,7 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 175975-76:
(8*1)+(7*7)+(6*5)+(5*9)+(4*7)+(3*5)+(2*7)+(1*6)=195
195 % 10 = 5
So 175975-76-5 is a valid CAS Registry Number.

175975-76-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-methoxy-1-(2-methylpropyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole

1.2 Other means of identification

Product number -
Other names 1-isobutyl-7-methoxy-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole

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:175975-76-5 SDS

175975-76-5Upstream product

175975-76-5Downstream Products

175975-76-5Relevant articles and documents

Tandem intramolecular photocycloaddition-retro-mannich fragmentation as a route to spiro[pyrrolidine-3,3′-oxindoles]. Total synthesis of (±)-coerulescine, (±)-horsfiline, (±)-elacomine, and (±)-6-deoxyelacomine

White, James D.,Li, Yang,Ihle, David C.

experimental part, p. 3569 - 3577 (2010/07/04)

Figure presented Irradiation of a tryptamine linked through its side-chain nitrogen to an alkylidene malonate residue results in an intramolecular [2 + 2] cycloaddition to the indole 2,3-double bond. The resultant cyclobutane undergoes spontaneous retro-M

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