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22424-58-4
4-(Benzyloxy)-2-methyl-1-nitrobenzene

Catalog#:1P003MVT

CAS:22424-58-4

MDL:MFCD00024269

Molecular Formula:C14H13NO3

Molecular Weight:243.2579

UN Number:

Haz Class:

Packing Group:

Synonyms: 5-Benzyloxy-2-nitrotoluene; 22424-58-4; AC1Q2ELF; Maybridge1_006779; ACMC-1CN6U; AC1L5XE5; AC1Q20EQ; Oprea1_658505; SCHEMBL1061802; CTK4E9461; Ether, benzyl 4-nitro-m-tolyl-; HMS560M03; 4-(Benzyloxy)-2-methyl-1-nitrobenzene; ZINC83383; 4-benzyloxy-2-methyl nitrobenzene; ACT09294; 4-benzyloxy-2-methyl-1-nitrobenzene; ANW-24866; CCG-40818; NSC-86149; BENZYL 4-NITRO-M-TOLYL ETHER; (3-Methyl-4-nitrophenyl)benzyl ether; AKOS015839415; 5-Benzoxy-2-nitrotoluene; MCULE-2523871101; VZ30064; AJ-10639; ZB002965; 4-(Benzyloxy)-2-methyl-1-nitrobenzene #; 2-methyl-1-nitro-4-(phenylmethoxy)benzene; DB-045909; TR-031238; FT-0620045; ST50407879; PBAXHOUGHZKSRP-UHFFFAOYSA-N; V4502; B-7995; SR-01000630933; Q-102046; SR-01000630933-1; SR-01000630933-2; I14-58106; 5-(Benzyloxy)-2-nitrotoluene; C14H13NO3; EINECS 244-988-3; MFCD00024269; AR-1G7315; C14-H13-N-O3; CID257720; 1-((3-methyl-4-nitrophenoxy)methyl)benzene; 5-Benzyloxy-2-nitrotoluene, 95% - 1G 1g; 25476-46-4; 2-methyl-1-nitro-4-phenylmethoxybenzene; Benzene,2-methyl-1-nitro-4-(phenylmethoxy)-; Benzene, 2-methyl-1-nitro-4-(phenylmethoxy)-; NSC86149;

Keywords: 22424-58-4,MFCD00024269,1P003MVT,4-(Benzyloxy)-2-methyl-1-nitrobenzene,C14H13NO3

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Catalog# Purity Size Price Dis. Price Availability Quantity
1P003MVT 97% 25g $33.00 $25.00 In Stock USA ADD TO CART BUY NOW 

  •                                        The compound 4-(Benzyloxy)-2-methyl-1-nitrobenzene has proven to be a valuable reagent in chemical synthesis due to its versatile properties. In organic synthesis, it serves as a key intermediate in the preparation of various pharmaceuticals, agrochemicals, and fine chemicals. One of the primary applications of 4-(Benzyloxy)-2-methyl-1-nitrobenzene is its role as a precursor in the synthesis of diverse compounds such as substituted benzenes, amines, and heterocyclic compounds. Its nitro group can undergo reduction reactions to yield primary aromatic amines, which are essential building blocks in the creation of complex organic molecules.Furthermore, the benzyloxy group in 4-(Benzyloxy)-2-methyl-1-nitrobenzene can be selectively removed under suitable conditions, allowing for the introduction of other functional groups at the desired positions on the aromatic ring. This flexibility makes it a valuable tool in designing and crafting new molecules with specific properties or functions.Overall, the strategic use of 4-(Benzyloxy)-2-methyl-1-nitrobenzene in chemical synthesis enables chemists to access a wide range of structurally diverse compounds, facilitating the discovery and development of novel materials and pharmaceutical agents.

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