56107-04-1 Usage
Description
3-(p-tert-butylphenyl)-2-methylpropanol, also known as Lyral, is a synthetic fragrance ingredient commonly used in personal care and household products. It is a colorless liquid with a floral and green scent that adds a fresh and clean aroma to various products. However, it is also known to be a skin allergen for some individuals and is used as a standard for testing allergenic potential in other compounds.
Uses
Used in Fragrance Industry:
3-(p-tert-butylphenyl)-2-methylpropanol is used as a fragrance ingredient for its floral and green scent, adding a fresh and clean aroma to personal care and household products.
Used in Allergenic Testing:
3-(p-tert-butylphenyl)-2-methylpropanol is used as a standard for testing allergenic potential in other compounds due to its known skin allergenic properties.
Used in Perfumes, Lotions, and Detergents:
Despite concerns about its potential to cause skin allergies, 3-(p-tert-but-butylphenyl)-2-methylpropanol is still found in a wide range of products such as perfumes, lotions, and detergents for its pleasant scent.
Check Digit Verification of cas no
The CAS Registry Mumber 56107-04-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,1,0 and 7 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 56107-04:
(7*5)+(6*6)+(5*1)+(4*0)+(3*7)+(2*0)+(1*4)=101
101 % 10 = 1
So 56107-04-1 is a valid CAS Registry Number.
InChI:InChI=1/C14H22O/c1-11(10-15)9-12-5-7-13(8-6-12)14(2,3)4/h5-8,11,15H,9-10H2,1-4H3
56107-04-1Relevant articles and documents
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Kogami,Kumanotani
, p. 3562,3565 (1973)
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Chemoselective hydrogenation of α,β-unsaturated aldehydes with modified Pd/C catalyst
Du, Wen Qiang,Rong, Ze Ming,Liang, Yan,Wang, Yong,Lu, Xin Yi,Wang, Yi Fan,Lu, Lian Hai
experimental part, p. 773 - 776 (2012/08/14)
Selective hydrogenation of α,β-unsaturated aldehydes with modified Pd/C catalyst was developed. The reduction of CO bond could be efficiently inhibited by the addition of carbonates, and high selectivity to the corresponding saturated aldehydes was achieved under mild conditions. This protocol provides an alternative for efficient preparation of saturated aldehydes.
Acid promoted CIDT for the deracemization of dihydrocinnamic aldehydes with Betti's base
Rosini, Goffredo,Paolucci, Claudio,Boschi, Francesca,Marotta, Emanuela,Righi, Paolo,Tozzi, Francesco
experimental part, p. 1747 - 1757 (2011/02/28)
Racemic α-epimerizable and unfunctionalized aldehydes have been converted into enantiomerically enriched mixtures through a sequence of (i) a conversion into the diastereoisomeric 3-substituted 1-phenyl-2,3-dihydro-1H- naphtho[1,2-e][1,3]oxazines by reaction with the (R)- or (S)-1-(α- aminobenzyl)-2-naphthol (Betti's base), (ii) an acid promoted crystallization-induced diastereoisomer transformation (CIDT), and (iii) a clean cleavage of the dihydro-1,3-naphthoxazinic ring of the enriched diastereoisomer, easily collected by filtration, allowing the recovery of the enantiomerically enriched aldehydes and the chiral auxiliary.