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35115-50-5

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35115-50-5 Usage

Explanation

Different sources of media describe the Explanation of 35115-50-5 differently. You can refer to the following data:
1. The compound's full name, which describes its structure and composition.
2. The compound is synthesized in the form of a hydrochloride salt, which is a common method for increasing the solubility and stability of certain compounds.
3. The compound's molecular structure consists of a core structure (chromeno[5,4,3-cde]chromene) with specific functional groups attached (dimethylaminoethyl and dimethoxy).
4. The compound has potential uses in the development of new pharmaceuticals and drugs, particularly in the study of biological processes and treatment of certain medical conditions.
5. The compound may be used as a research tool to help scientists better understand how it interacts with biological systems, which can provide valuable insights for drug development and other applications.
6. While the specific medical conditions are not mentioned in the material, the compound has the potential to be used in the treatment of various medical conditions due to its interactions with biological systems.
7. The hydrochloride salt form of the compound is likely to improve its solubility in water or other solvents, which can be important for its use in research and pharmaceutical applications.
8. The hydrochloride salt form may also enhance the stability of the compound, making it more suitable for use in various applications.

Primary Use

Research and medical laboratories

Synthesis

As a hydrochloride salt

Molecular Structure

Chromeno[5,4,3-cde]chromene core with dimethylaminoethyl and dimethoxy functional groups

Potential Applications

Pharmaceuticals and drug development

Role in Research

Tool for understanding interaction with biological systems

Medical Conditions

Treatment of certain medical conditions

Solubility

Increased by hydrochloride salt form

Stability

Enhanced by hydrochloride salt form

Check Digit Verification of cas no

The CAS Registry Mumber 35115-50-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,1,1 and 5 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 35115-50:
(7*3)+(6*5)+(5*1)+(4*1)+(3*5)+(2*5)+(1*0)=85
85 % 10 = 5
So 35115-50-5 is a valid CAS Registry Number.

35115-50-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name Taspin hydrochloride

1.2 Other means of identification

Product number -
Other names Taspinhydrochlorid

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:35115-50-5 SDS

35115-50-5Upstream product

35115-50-5Downstream Products

35115-50-5Relevant articles and documents

(-)-MAGLIFLOENONE, A NOVEL SPIROCYCLOHEXADIENONE NEOLIGNAN AND OTHER CONSTITUENTS FROM MAGNOLIA LILIFLORA

Talapatra, Bani,Chaudhuri, Prabir K.,Talapatra, Sunil K.

, p. 747 - 750 (1982)

A new neolignan designated (-)-maglifloenone and the known one futoenone, both of which contain the rarely occurring spirocyclohexadienone skeleton, have been isolated together with the tetrahydrofuranolignan (+)-veraguensin, an optically inactive tertiary base taspine and β-sitosterol from the leaves and twigs of Magnolia liliflora.The structure and stereochemistry of (-)-maglifloenone have been deduced from the spectral data and the mass fragmentation of (-)-maglifloenone and futoenone have been rationalized.This is the first report of two neolignans of spirocyclohexadienone skeleton an d of taspine from the Magnoliaceae family and the second report of the natural occurrence of futoenone.Key Word Index - Magnolia liliflora; Magnoliaceae; tetrahydrofuranolignan; (+)-veraguensin; neolignans; futoenone; (-)-maglifloenone; aporphine derived alkaloid; taspine; β-sitosterol; mass spectral study.

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