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Benzenemethanol, 4-(1,1-dimethylethyl)-α-[4-(1,1-dimethylethyl)phenyl]-, also known as 4-tert-butylbenzyl alcohol or 4-(4-tert-butylphenyl)-2-methyl-2-butanol, is an organic compound with the molecular formula C15H24O. It is a colorless liquid with a molecular weight of 220.35 g/mol. Benzenemethanol, 4-(1,1-dimethylethyl)-a-[4-(1,1-dimethylethyl)phenyl]- is characterized by the presence of a benzyl alcohol group (C6H5-CH2OH) and two tert-butyl groups (C(CH3)3) attached to the benzene ring. It is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. The compound is also known for its antioxidant properties and is used in the stabilization of polymers. It is typically synthesized through the reduction of 4-tert-butylbenzaldehyde or through the Friedel-Crafts alkylation of 4-tert-butylbenzene with 2-methyl-2-butene.

16607-60-6

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16607-60-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16607-60-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,6,0 and 7 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 16607-60:
(7*1)+(6*6)+(5*6)+(4*0)+(3*7)+(2*6)+(1*0)=106
106 % 10 = 6
So 16607-60-6 is a valid CAS Registry Number.

16607-60-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name bis(4-tert-butylphenyl)methanol

1.2 Other means of identification

Product number -
Other names 4,4'-Di-tert-butyl-benzhydrol

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:16607-60-6 SDS

16607-60-6Relevant academic research and scientific papers

Trivalent Rare-Earth Metal Amide Complexes as Catalysts for the Hydrosilylation of Benzophenone Derivatives with HN(SiHMe2)2 by Amine-Exchange Reaction

Shinohara, Koichi,Tsurugi, Hayato,Anwander, Reiner,Mashima, Kazushi

supporting information, p. 14130 - 14136 (2020/10/06)

The rare-earth metal complexes Ln(L1)[N(SiHMe2)2](thf) (Ln=La, Ce, Y; L1=N,N′′-bis(pentafluorophenyl)diethylenetriamine dianion) were synthesized by treating Ln[N(SiHMe2)2]3(thf)2 with L1H2. The lanthanum and cerium derivatives are active catalysts for the hydrosilylation of benzophenone derivatives with HN(SiHMe2)2. An amine-exchange reaction was revealed as a key step of the catalytic cycle, in which Ln?Si?H β-agostic interactions are proposed to promote insertion of the carbonyl moiety into the Si?H bond.

Dual Nickel- And Photoredox-Catalyzed Reductive Cross-Coupling of Aryl Halides with Dichloromethane via a Radical Process

Xu, Tao,Xu, Wenhao,Zheng, Purui

supporting information, (2020/11/13)

The first catalytic strategy to harness a new chloromethane radical from dichloromethane under dual Ni/photoredox catalytic conditions has been developed. Compared with traditional two-electron reductive process associated with metallic reductants, this method via a single-electron approach can proceed under exceptionally mild conditions (visible light, ambient temperature, no strong base) and exhibits complementary reactivity patterns. It affords a broad scope of many functional groups, including alkenyl, which suffers cyclopropanation in previous routes. The diarylmethane-d2 compounds can be readily available with this transformation.

Structure-based virtual screening, synthesis and biological evaluation of potential FAK-FAT domain inhibitors for treatment of metastatic cancer

Hiscox, Stephen E.,Jones, Samuel R.,Kandil, Sahar B.,Smith, Sonia,Westwell, Andrew D.

, (2020/08/28)

Focal adhesion kinase (FAK) is a tyrosine kinase that is overexpressed and activated in several advanced-stage solid cancers. In cancer cells, FAK promotes the progression and metastasis of tumours. In this study, we used structure-based virtual screening to filter a library of more than 210K compounds against the focal adhesion targeting FAK-focal adhesion targeting (FAT) domain to identify 25 virtual hit compounds which were screened in the invasive breast cancer line (MDA-MB-231). Most notably, compound I showed low micromolar antiproliferative activity, as well as antimigratory activity. Moreover, examination in a model of triple negative breast cancer (TNBC), revealed that, despite not effecting FAK phosphorylation, compound I significantly impairs proliferation whilst impairing focal adhesion growth and turnover leading to reduced migration. Further optimisation and synthesis of analogues of the lead compound I using a four-step synthetic procedure was performed, and analogues were assessed for their antiproliferative activity against three breast cancer (MDA-MB-231, T47D, BT474) cell lines and one pancreatic cancer (MIAPaCa2) cell line. Compound 5f was identified as a promising lead compound with IC50 values in the range of 4.59–5.28 μM in MDA-MB-231, T47D, BT474, and MIAPaCa2. Molecular modelling and pharmacokinetic studies provided more insight into the therapeutic features of this new series.

Chiral gating for size- And shape-selective asymmetric catalysis

Li, Xiaowei,Zhao, Yan

supporting information, p. 13749 - 13752 (2019/08/26)

A poor or mediocre stereoselectivity is a key roadblock for a chiral catalyst to find practical adoptions. We report a facile method to create a tunable chiral space near a chiral catalyst to augment its selectivity. The space was created rationally throu

Large-scale synthesis of novel sterically hindered acenaphthene-based α-diimine ligands and their application in coordination chemistry

Guo, Lihua,Kong, Wenyu,Xu, Yanjian,Yang, Yuliang,Ma, Rui,Cong, Li,Dai, Shengyu,Liu, Zhe

supporting information, p. 58 - 67 (2018/02/14)

An efficient method to synthesize novel highly sterically hindered acenaphthene-based α-diimine ligands bearing bulky diarylmethyl moiety was achieved by two-step reactions. These reactions could be carried out on a scale of 100 g with no chromatography involved. On the basis of this method, a series of novel highly sterically hindered acenaphthene-based α-diimine Pd(II) and Ni(II) complexes, imidazolium precursors and the corresponding NHCs-metal complexes were also successfully synthesized. These novel complexes can offer great potential for metal-catalyzed polymerizations and organic reactions.

[Pd(IPr*R)(acac)Cl]: Efficient bulky Pd-NHC catalyst for Buchwald-Hartwig C-N cross-coupling reaction

Tian, Xiabing,Lin, Jing,Zou, Sheng,Lv, Junwei,Huang, Qingfei,Zhu, Jin,Huang, Shuping,Wang, Qiwei

supporting information, p. 125 - 130 (2018/03/06)

A series of bulky palladium catalysts based on N-heterocyclic carbene, (Pd(NHC)(acac)Cl: NHC = IPr*me = N,N′-bis(2,6-bis(di-p-tolylmethyl)-4-methylphenyl)-imidazol-2 -ylidene, Pd(IPr*me)(acac)Cl; NHC = IPr*ipr = N,N′-bis(2,6-bis(di-4-isopropylphenyl)-4-methylphenyl)-imidazol-2 -ylidene, Pd(IPr*ipr)(acac)Cl; and NHC = IPr*tBu = N,N′-bis(2,6-bis(di-4-(tert-butyl)phenyl)- 4-methylphenyl)- imidazol-2-ylidene, Pd(IPr*tBu)(acac)Cl; acac = acetylacetonate), have been designed and synthesized. These three new catalysts showed much better catalytic activity in the Buchwald?Hartwig arylamination coupling reaction as compare to the earlier congener (IPr*)Pd(acac)Cl (IPr* = N,N′-bis(2,6-diphenylmethyl)-4-methylphenylimidazol-2-ylidene). The highly active PdII precatalyst [Pd(IPr*me)(acac)Cl] has been fully explored by using a wide range of substrates with different electronic and steric demands of coupling partners, for which up to 99% isolated yields were obtained. Remarkably, the moderate isolated yield was obtained for the challenging coupling of the amine bearing very bulky groups.

Acenequinocumulenes: Lateral and Vertical π-Extended Analogues of Tetracyanoquinodimethane (TCNQ)

Gruber, Marco,Padberg, Kevin,Min, Jie,Waterloo, Andreas R.,Hampel, Frank,Maid, Harald,Ameri, Tayebeh,Brabec, Christoph J.,Tykwinski, Rik R.

supporting information, p. 17829 - 17835 (2017/11/27)

We have designed a series of molecules and developed synthetic methodology that allows for the inclusion of structural diversity along both the lateral and vertical axes of the basic TCNQ skeleton. In the lateral direction, benzoannulation extends the π-s

Visible light-mediated arylalkylation of allylic alcohols through concomitant 1,2-aryl migration

Huang, Hong-Li,Yan, Hang,Yang, Chao,Xia, Wujiong

supporting information, p. 4910 - 4913 (2015/03/18)

A photocatalytic process for selective arylalkylation of allylic alcohols with α-bromo diethyl malonate has been developed. The reaction provided a straightforward approach to synthesize α-aryl-β-alkylated ketones via unique 1,2-aryl migration. The procedure is highlighted by its operational simplicity and mild reaction conditions.

UV light-mediated difunctionalization of alkenes through aroyl radical addition/1,4-/1,2-Aryl shift cascade reactions

Zheng, Lewei,Huang, Hongli,Yang, Chao,Xia, Wujiong

supporting information, p. 1034 - 1037 (2015/03/30)

UV light-mediated difunctionalization of alkenes through an aroyl radical addition/1,4-/1,2-aryl shift has been described. The resulted aroyl radical from a photocleavage reaction added to acrylamide compounds followed by cyclization led to the formation of oxindoles, whereas the addition to cinnamic amides aroused a unique 1,4-aryl shift reaction. Furthermore, the difunctionalization of alkenes of prop-2-en-1-ols was also achieved through aroyl radical addition and a sequential 1,2-aryl shift cascade reaction.

Dual gold catalysis: Synthesis of polycyclic compounds via C-H insertion of gold vinylidenes

Wieteck, Marcel,Tokimizu, Yusuke,Rudolph, Matthias,Rominger, Frank,Ohno, Hiroaki,Fujii, Nobutaka,Hashmi, A. Stephen K.

supporting information, p. 16331 - 16336 (2015/01/09)

New and interesting polycyclic compounds have been synthesized from non-conjugated diyne systems by dual gold catalysis. A quaternary carbon center in the backbone and the accompanying Thorpe-Ingold effect enabled the unprecedented insertion of sp3 and sp2 C-H bonds that for the first time were incorporated within the backbone of the diyne system and allowed the construction of complex polycyclic carbon scaffolds inaccessible by previous approaches in which the C-H bonds for the insertion were situated at the other end of the alkyne.

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