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51503-08-3
4-tert-Butoxybenzyl Alcohol

Catalog#:1P003MHY

CAS:51503-08-3

MDL:MFCD00082599

Molecular Formula:C11H16O2

Molecular Weight:180.2435

UN Number:

Haz Class:

Packing Group:

Synonyms: 51503-08-3; 4-tert-Butoxybenzyl alcohol; EINECS 257-246-9; AC1MI3GJ; 4-(tert-Butoxy)benzylalcohol; H9N2O3P; SCHEMBL319906; CTK4J4372; DTXSID40199487; ZINC2572161; 7181AB; 7182AB; (4-(tert-Butoxy)phenyl)methanol; CL8733; RW1233; AKOS015995794; AB03109; AM84234; TRA0055201; 1-tert-butoxy-4-(hydroxymethyl)benzene; ACM51503083; AJ-41971; AN-41227; (4-TERT-BUTOXY-PHENYL)-METHANOL; AS-46091; Benzenemethanol,4-(1,1-dimethylethoxy)-; CJ-09932; SC-54485; SY015586; AB0066544; AX8046025; DB-071362; TC-030951; FT-0080757; p-tert-Butoxybenzyl alcohol; FT-0650943; 4-(1,1-DIMETHYLETHOXY)BENZENEMETHANOL; Z-4326; MFCD00082599 (97+%); C-56845; -methanol; Ammonium hydrogenphosphite; C11H16O2; C11-H16-O2; CID3016675; (4-TERT-BUTOXYPHENYL)METHANOL; 877-65-6; 1019021-85-2; 51503-61-8; 4-(TERT-BUTOXY)BENZYL ALCOHOL; 4-T-BUTOXYBENZYL ALCOHOL; Benzenemethanol, 4-(1,1-dimethylethoxy)-; [4-[(2-methylpropan-2-yl)oxy]phenyl]methanol;

Keywords: 51503-08-3,MFCD00082599,1P003MHY,4-tert-Butoxybenzyl Alcohol,C11H16O2

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Catalog# Purity Size Price Dis. Price Availability Quantity
1P003MHY 95% 250mg $127.00 $95.00 In Stock USA ADD TO CART BUY NOW
1P003MHY 95% 1g $207.00 $155.00 In Stock USA ADD TO CART BUY NOW

  • 4-tert-Butoxybenzyl Alcohol, also known as TBBA, is a versatile compound widely used in chemical synthesis as a protecting group for hydroxyl groups. This compound plays a crucial role in organic chemistry by temporarily masking the hydroxyl functionality of various compounds, providing protection from undesired reactions during synthetic processes. The tert-butoxybenzyl protecting group can be selectively removed under mild acidic conditions, allowing for further modification of the target molecule. Due to its stability and ease of removal, 4-tert-Butoxybenzyl Alcohol is favored in the synthesis of complex organic molecules and pharmaceuticals. It enables chemists to control the reactivity of hydroxyl groups, facilitating efficient and selective transformations in multi-step synthesis strategies.

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