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2915-44-8

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2915-44-8 Usage

Chemical structure

Two 4-azidobenzene groups linked by a methylene bridge

Physical appearance

White to light grey crystalline solid

Primary use

Cross-linking agent in the production of high performance polymers (e.g., polyimides and polybenzoxazines)

Additional uses

Synthesis of azido-substituted compounds, photoinitiator in photopolymerization reactions

Safety concerns

Potentially explosive, toxic effects on the respiratory system if inhaled in high concentrations

Safety precautions

Handle with care, follow proper safety measures when working with the compound

Check Digit Verification of cas no

The CAS Registry Mumber 2915-44-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,1 and 5 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2915-44:
(6*2)+(5*9)+(4*1)+(3*5)+(2*4)+(1*4)=88
88 % 10 = 8
So 2915-44-8 is a valid CAS Registry Number.

2915-44-8SDS

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 1,1'-Methylenebis(4-azidobenzene)

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:2915-44-8 SDS

2915-44-8Relevant articles and documents

Chemistry of Tetradentate [C,N : C,N] Iminophosphorane Palladacycles: Preparation, Reactivity and Theoretical Calculations

Munín-Cruz, Paula,Ortigueira, Juan M.,Pereira, M. Teresa,Rúa-Sueiro, Marcos,Reigosa, Francisco,Vila, José M.

, p. 1190 - 1194 (2020)

A theoretical and experimental study of tetradentate [C,N : C,N] iminophosphorane palladacycles was carried out for the purpose of elucidating their behavior as compared to the parent Schiff base analogues to determine the prospect of encountering new A-frame structures for the iminophosphorane derivatives. The DFT calculations were in agreement with the experimental results regarding the performance of these ligands. New insights into the chemistry of the related dinuclear species have been obtained.

Synthesis and insecticidal activity of N,N'-bis (3-substituted thiourea) methylenedianiline derivatives

Sravanthi,Pottem, Madhusudhana Reddy,Manju

, p. 77 - 80 (2013/12/04)

Bis thiourea derivatives (5a-e) were synthesized by the treatment of diisothiocyanate (4) with various secondary amines and anilines. The structures of the compounds (5a- e) were confirmed by their spectral analysis. The insecticidal activity of the diisothicoyanate (4) and bisthiourea derivatives (5a-e) were studied and found to be better activities in comparison with the standard drug.

Size-specific ligands for RNA hairpin loops

Thomas, Jason R.,Liu, Xianjun,Hergenrother, Paul J.

, p. 12434 - 12435 (2007/10/03)

The targeting of one mRNA in the transcriptome requires small molecules that bind with substantial affinity and specificity. As such, compounds with specificity for individual RNA secondary structural motifs could be useful for targeting RNA. Described herein is the synthesis of a combinatorial library of 105 dimers of deoxystreptamine and the subsequent identification of compounds with specificity for specific RNA hairpin loop sizes, including tetraloops and octaloops. Such compounds will be useful for the perturbation of RNA function in vivo. Copyright

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