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4371-35-1

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4371-35-1 Usage

General Description

"1,1'-Biphenyl]-2,2',6,6'-tetrol" is a chemical compound known for its unique molecular structure comprised of two benzene rings that are connected by a single carbon-carbon bond. This comprehensive structure makes it a key ingredient in various industrial and scientific applications. It belongs to the class of organic compounds known as biphenyls and derivatives. These are organic compounds containing to phenyl groups linked together by a C-C bond. Although it presents significant interest, little is known about its toxicity and environmental impacts due to the lack of extensive research. Thus, handling it requires strict safety measures to reduce potential health risks and environmental harm.

Check Digit Verification of cas no

The CAS Registry Mumber 4371-35-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,7 and 1 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4371-35:
(6*4)+(5*3)+(4*7)+(3*1)+(2*3)+(1*5)=81
81 % 10 = 1
So 4371-35-1 is a valid CAS Registry Number.

4371-35-1Downstream Products

4371-35-1Relevant articles and documents

Selective Rhodium-Catalyzed Hydroformylation of Terminal Arylalkynes and Conjugated Enynes to (Poly)enals Enabled by a π-Acceptor Biphosphoramidite Ligand

Zhao, Jiangui,Zheng, Xueli,Tao, Shaokun,Zhu, Yuxin,Yi, Jiwei,Tang, Songbai,Li, Ruixiang,Chen, Hua,Fu, Haiyan,Yuan, Maolin

supporting information, p. 6067 - 6072 (2021/08/16)

The hydroformylation of terminal arylalkynes and enynes offers a straightforward synthetic route to the valuable (poly)enals. However, the hydroformylation of terminal alkynes has remained a long-standing challenge. Herein, an efficient and selective Rh-catalyzed hydroformylation of terminal arylalkynes and conjugated enynes has been achieved by using a new stable biphosphoramidite ligand with strong π-acceptor capacity, which affords various important E-(poly)enals in good yields with excellent chemo- and regioselectivity at low temperatures and low syngas pressures.

Hydroxylated biphenyls as tyrosinase inhibitor: A spectrophotometric and electrochemical study

Ruzza, Paolo,Serra, Pier Andrea,Fabbri, Davide,Dettori, Maria Antonietta,Rocchitta, Gaia,Delogu, Giovanna

supporting information, p. 1034 - 1038 (2016/12/26)

A small collection of C2-symmetry hydroxylated biphenyls was prepared by straightforward methods and the capability to act as inhibitors of tyrosinase has been evaluated by both spectrophotometric and electrochemical assays. Our attention was f

P(O)R2-directed Pd-catalyzed C-H functionalization of biaryl derivatives to synthesize chiral phosphorous ligands

Hu, Rong-Bin,Wang, Hong-Li,Zhang, Hong-Yu,Zhang, Heng,Ma, Yan-Na,Yang, Shang-Dong

supporting information, p. 2071 - 2076 (2014/11/08)

Chiral phosphorus ligands have been widely used in transition metal-catalyzed asymmetric reactions. Herein, we report a new synthesis approach of chiral biaryls containing a phosphorus moiety using P(O)R 2-directed Pd-catalyzed C-H activation; the functionalized products are produced with good enantioselectivity.

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