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5-BROMO-2-(PROP-2-YNYLOXY)BENZALDEHYDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

122835-14-7

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122835-14-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 122835-14-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,8,3 and 5 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 122835-14:
(8*1)+(7*2)+(6*2)+(5*8)+(4*3)+(3*5)+(2*1)+(1*4)=107
107 % 10 = 7
So 122835-14-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H7BrO2/c1-2-5-13-10-4-3-9(11)6-8(10)7-12/h1,3-4,6-7H,5H2

122835-14-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-bromo-2-prop-2-ynoxybenzaldehyde

1.2 Other means of identification

Product number -
Other names 5-bromo-2-(prop-2-ynyloxy)benzaldehyde

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:122835-14-7 SDS

122835-14-7Relevant academic research and scientific papers

Efficient one pot synthesis of chromenonaphthyridine derivatives by CuI/InCl3 catalyzed aza diels-alder reaction

Maji, Pradip Kumar,Mahalanobish, Ayan

, p. 42 - 49 (2018)

A mild and efficient method for the synthesis of chromenonaphthyridine derivatives via domino reaction of aminopyridine and different O-propargylated salicylaldehydes using CuI/InCl3 as an efficient catalyst, refluxed in acetonitrile is reported. Mild rea

Synthesis and biological properties of novel 1-methyl-2-(2-(prop-2-yn-1-yloxy)benzylidene) hydrazine analogues

Kivrak, Arif,Yilmaz, Can,Konus, Metin,Koca, Halil,Aydemir, Selahattin,Oagaz, Jeger Ali

, p. 306 - 316 (2018)

1-Methyl-2-(2-(prop-2-yn-1-yloxy)benzylidene)hydrazine analogues were readily prepared in good yields by the reaction of 2-(prop-2-yn-1-yloxy)benzaldehydes and methyl hydrazine. The reaction tolerates a variety of substituents on the 2-hydroxybenzaldehyde

Synthesis of coumarin-sulfonamide derivatives and determination of their cytotoxicity, carbonic anhydrase inhibitory and molecular docking studies

Zengin Kurt, Belma,Sonmez, Fatih,Ozturk, Dilek,Akdemir, Atilla,Angeli, Andrea,Supuran, Claudiu T.

, (2019)

Carbonic anhydrases isoforms CA IX, and XII are known to be highly expressed in various human tissues and malignancies. CA IX is a prominent target for especially colorectal cancers, because it is overexpressed in colorectal cancer and this overexpression

Synthesis of new benzo[f]imidazo[1,2-d][1,4]oxazepines: AgNO3-mediated intramolecular hydroamination

Mahdavi, Mohammad,Hariri, Roshanak,Saeedi, Mina,Foroumadi, Alireza,Shafiee, Abbas,Akbarzadeh, Tahmineh

, p. 7082 - 7084 (2015)

Novel benzo[f]imidazo[1,2-d][1,4]oxazepine derivatives were synthesized from [4,5-diaryl-2-(2-(prop-2-yn-1-yloxy)aryl)-1H-imidazoles] by a AgNO3-promoted 7-exo-dig hydroamination proceeding in DMF at 80 °C.

Efficient synthesis of novel 1, 2, 3-triazole-based diazepam derivatives by click CuAAC reaction: Spectroscopic characterizations and DFT studies

Esmaeeli, Zohreh,Khodabakhshi, Mohammad Reza,Mirjafary, Zohreh,Saeidian, Hamid

, (2021)

A new family of 1, 2, 3-triazole-based benzodiazepines have been synthesized by the Huisgen [3+2] dipolar cycloaddition reaction of diazepam with O-propargyl salicylaldehydes in the aqueous medium. Mild reaction conditions, excellent yields (70–98%), envi

Coumarin-1,2,3-triazole hybrid derivatives: Green synthesis and DFT calculations

Nouraie, Pegah,Moradi Dehaghi, Shahram,Foroumadi, Alireza

, p. 386 - 394 (2019)

A series of new 1,2,3-triazole-coumarin hybrid system are synthesized from the click reaction between 3-azido coumarin and different aromatic terminal alkyne derivatives in a green manner. All compounds are characterized by IR, NMR and UV–VIS spectroscopy

Synthesis and spectral study of a new family of 2,5-diaryltriazoles having restricted rotation of the 5-aryl substituent

Tsyrenova, Biligma,Nenajdenko, Valentine

, (2020)

Efficient synthesis of 2,5-diaryl substituted 4-azido-1,2,3-triazoles by the reaction of sodium azide with dichlorosubstituted diazadienes was demonstrated. The optical properties of the prepared azidotriazoles were studied to reveal a luminescence maximu

Synthesis of Novel 7-methylene-6,7-dihyrobenzo[f]Benzo[4,5]Imidazo[1,2-d][1,4]Oxazepines via Base-mediated Regioselective Intramolecular Hydroamination

Yavari, Hossein,Alinezhad, Heshmatollah,Shafiee, Abbas

, p. 2393 - 2396 (2017)

A versatile and transition metal-free approach for the synthesis of new 7-methylene-6,7-dihyrobenzo[f]benzo[4,5]imidazo[1,2-d][1,4]oxazepines were developed by an efficient 7-exo-dig regioselective hydroamination of 2-(2-(prop-2-yn-1-yloxy)phenyl)-1H-benzo[d]imidazole in the presence of potassium carbonate in DMF at 90°C.

Synthesis and evaluation of novel triazoles and mannich bases functionalized 1,4-dihydropyridine as angiotensin converting enzyme (ACE) inhibitors

Kumbhare, Ravindra M.,Kosurkar, Umesh B.,Bagul, Pankaj K.,Kanwal, Abhinav,Appalanaidu,Dadmal, Tulshiram L.,Banerjee, Sanjay Kumar

, p. 5824 - 5830 (2014)

A series of novel diethyl 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate embedded triazole and mannich bases were synthesized, and evaluated for their angiotensin converting enzyme (ACE) inhibitory activity. Screening of above synthesized compounds fo

Synthesis, characterization, PASS prediction and in silico ADME studies of ester and ether linked 1,4-disubstituted 1,2,3-triazoles derivatives via click approach

Krishnaswamy,Raghuram Shetty,Roopa,Banu, Salma,Preritha,Rajeshwari,Ravikumar,Pruthviraj,Aruna Kumar,Sreenivasa

, p. 1857 - 1864 (2020)

In the present investigation, we focused our interest on the synthesis of pharmacophoric units (quinoline and 1,2,3-triazole) linked through ester (3a-b) and (substituted aromatic ring and 1,2,3-triazole) linked through an ether (3c-h). The synthesis invo

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