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181034-50-4

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181034-50-4 Usage

Molecular Structure

A complex structure with a fused indeno[1,2-b]pyrazine ring system.

Isomerism

A trans-isomer, indicating the spatial arrangement of the molecular components.

Hydrocarbon Chain

Contains a hexahydro (six hydrogen atoms) chain.

Substitution

A 1-methyl group is attached to the molecule.

Potential Applications

Possible uses in organic synthesis or pharmaceutical research.

Research Status

Requires further research and testing to understand its potential uses and effects.

Check Digit Verification of cas no

The CAS Registry Mumber 181034-50-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,1,0,3 and 4 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 181034-50:
(8*1)+(7*8)+(6*1)+(5*0)+(4*3)+(3*4)+(2*5)+(1*0)=104
104 % 10 = 4
So 181034-50-4 is a valid CAS Registry Number.

181034-50-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (4aS,9aS)-1-Methyl-2,3,4,4a,9,9a-hexahydro-1H-indeno[1,2-b]pyrazi ne

1.2 Other means of identification

Product number -
Other names -

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:181034-50-4 SDS

181034-50-4Downstream Products

181034-50-4Relevant articles and documents

Stereoselective Construction of Vicinal Diamines. Part 2. Synthesis of Indenopyrazines

Orlek, Barry S.,Lightowler, Diane

, p. 1307 - 1312 (1993)

The trans-adduct 8 derived from indene and N,N-dichlorourethane serves as a precursor for the cis-1,2-diaminoindane 6 and the trans-diamines 7 and 14.Conversion of 6 and 14 into the triazabenzocycloheptafluorenes 1 and 2, respectively, via the indenopyrazines 4 and 5 is described.

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