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100-83-4
Benzaldehyde, 3-hydroxy-

Catalog#:1P0000OK

CAS:100-83-4

MDL:MFCD00003368

Molecular Formula:C7H6O2

Molecular Weight:122.1213

UN Number:

Haz Class:

Packing Group:

Synonyms: 3-hydroxybenzaldehyde; m-hydroxybenzaldehyde; Benzaldehyde, m-hydroxy-; 3-HYDROXY-BENZALDEHYDE; UNII-8Z2819J40E; 3-hydroxy benzaldehyde; NSC 3504; EINECS 202-892-9; MFCD00003368; BRN 0507099; AI3-12120; CHEBI:16207; meta-hydroxybenzaldehyde; IAVREABSGIHHMO-UHFFFAOYSA-N; 8Z2819J40E; 3-Hydroxybenzaldehyde, 98.5%; 3-Hydroxybenzaldehyd; 3-hydroxylbenzaldehyde; 3-oxidanylbenzaldehyde; m-hydroxy benzaldehyde; PubChem7767; 3-hydroxy benzoaldehyde; (3-hydroxyphenyl)methanone; 3-hydroxybenzaldehyde; ACMC-2097so; EC 202-892-9; AC1L18HC; SCHEMBL35726; 4-08-00-00240 (Beilstein Handbook Reference); KSC177G0R; (3-hydroxyphenyl) formaldehyde; AC1Q790K; CHEMBL243816; Jsp000165; 100-83-4; 3-Hydroxybenzaldehyde, >=99%; DTXSID7059220; CTK0H7308; NSC3504; ZINC901630; ACT07002; CS-M0589; KS-000002LQ; NSC-3504; STR01419; m-Formylphenol; ANW-14374; BBL022923; CH0044; SBB040208; STK199259; AKOS000119743; AC-1263; AN-7017; LS10593; MCULE-7122569137; m-Hydroxybenzaldehyde; RP19454; RP19455; RTR-000254; TRA0025040; AJ-24373; AK-77369; BC226069; CJ-04551; LS-25059; SC-00058; 3-Formylphenol; SY001091; ZB015296; AB1002514; ST2410731; TR-000254; FT-0615830; ST50213351; A-7626; C03067; H-3750; Benzaldehyde, 3-hydroxy-; 12829-EP2295414A1; 12829-EP2316831A1; MFCD00003368 (97+%); I01-1978; F2190-0629; InChI=1/C7H6O2/c8-5-6-2-1-3-7(9)4-6/h1-5,9; 3-Hydroxybenzaldehyde, purum, >=95.0% (HPLC), faintly yellow to light brown; null; Ethyl glyoxalate; Benzaldehido, 3-hidroxi-; meta-Hydroxybenzaldehyde; C7H6O2; CID101; 3-Hydroxybenzaldehyde, 97% 25g; C7-H6-O2; c0055; ACN-040335; H0197; 3-Hydroxybenzaldehyde, 99% - 100G 100g; C011275; 924-44-7;

Keywords: 100-83-4,MFCD00003368,1P0000OK,Benzaldehyde, 3-hydroxy-,C7H6O2

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Catalog# Purity Size Price Dis. Price Availability Quantity
1P0000OK 98% 10g $6.00 $4.00 In Stock USA ADD TO CART BUY NOW
1P0000OK 98% 25g $7.00 $6.00 In Stock USA ADD TO CART BUY NOW
1P0000OK 98% 100g $11.00 $9.00 In Stock USA ADD TO CART BUY NOW
1P0000OK 98% 500g $51.00 $39.00 In Stock USA ADD TO CART BUY NOW

  • Benzaldehyde, 3-hydroxy-, also known as o-hydroxybenzaldehyde, is a versatile chemical that plays an important role in organic synthesis. It acts as a building block for various chemical compounds due to its aromatic aldehyde group and the reactive hydroxy group on the benzene ring.
    
    One of its primary applications is in the synthesis of flavor and fragrance chemicals. The aldehyde group can undergo condensation reactions with various organic compounds to form imines and Schiff bases, which are used as intermediates in the production of more complex molecules that are typical in the flavor and perfumery industry.
    
    Moreover, 3-hydroxybenzaldehyde serves as a precursor to synthetic pharmaceuticals. It can be used to create compounds with potential medicinal properties such as anti-inflammatory, antimicrobial, and anticancer agents. For instance, it can be employed in the formation of flavonoids, which exhibit a range of biological activities and are used as dietary supplements.
    
    In polymer chemistry, 3-hydroxybenzaldehyde is valuable due to its capacity to form phenolic resins, which possess high thermal stability and mechanical strength. These resins may find applications in the construction of molded products and as binders in composite materials.
    
    Additionally, this compound is useful in the field of organic electronics, particularly in the synthesis of certain types of organic semiconductors that require phenolic precursors. Organic semiconductors are integral in the development of flexible electronic devices.
    
    Furthermore, in the realm of dyes and pigments, 3-hydroxybenzaldehyde can be used to synthesize certain azo dyes and related organic compounds that confer color properties necessary for fabric coloring applications.
    
    In organic chemistry, the hydroxyl group can be protected and then deprotected, allowing for chemoselective transformations on the aldehyde group. This property is essential for constructing complex molecules in a step-wise and controlled manner.
    
    Lastly, in research, it is employed as a reagent to investigate the mechanistic pathways of various chemical reactions due to its easily modifiable structure. It is particularly important in the study of photochemical processes and as a substrate in catalysis research.
    
    Overall, benzaldehyde, 3-hydroxy-, with its reactive functional groups, offers a pathway for the synthesis of a wide array of chemical products, proving its integral role in chemical synthesis and industrial applications.

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