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134456-76-1

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134456-76-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 134456-76-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,4,5 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 134456-76:
(8*1)+(7*3)+(6*4)+(5*4)+(4*5)+(3*6)+(2*7)+(1*6)=131
131 % 10 = 1
So 134456-76-1 is a valid CAS Registry Number.

134456-76-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-iodophenyl)phenylmethanol

1.2 Other means of identification

Product number -
Other names o-iodophenylbenzyl alcohol

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:134456-76-1 SDS

134456-76-1Relevant articles and documents

o-Trimethylsilylphenyllithium as a synthetic equivalent of o-halophenyllithium

Takahashi, Masaki,Hatano, Ken,Kimura, Mikio,Watanabe, Toshinari,Oriyama, Takeshi,Koga, Gen

, p. 579 - 582 (1994)

The reaction of o-trimethylsilylphenyllithium with carbonyl compounds and subsequent halogenodesilylation with ICl afforded o-iodophenylcarbinols in good yields, showing the usefulness of o-trimethylsilylphenyllithium as a synthetic equivalent of o-iodophenyl anion. The reaction via a protected o-trimethylsilylphenylcarbinol is also shown.

Highly Enantioselective Cobalt-Catalyzed Hydroboration of Diaryl Ketones

Liu, Wenbo,Guo, Jun,Xing, Shipei,Lu, Zhan

supporting information, p. 2532 - 2536 (2020/04/02)

A highly enantioselective cobalt-catalyzed hydroboration of diaryl ketones with pinacolborane was developed using chiral imidazole iminopyridine as a ligand to access chiral benzhydrols in good to excellent yields and ee. This protocol could be carried out in a gram scale under mild reaction conditions with good functional group tolerance. Chiral biologically active 3-substituted phthalide and (S)-neobenodine could be easily constructed through asymmetric hydroboration as a key step.

Nitrogen-Iodine Exchange of Diaryliodonium Salts: Access to Acridine and Carbazole

Wang, Ming,Fan, Qiaoling,Jiang, Xuefeng

supporting information, p. 216 - 219 (2018/01/17)

A nitrogen-iodine exchange protocol of diaryliodonium salts with sodium azide salt is developed for general construction of significant functional acridines and carbazoles, in which introduction of nitrogen at a late stage was successfully established avoiding heteroatom incompatibility. Inorganic sodium azide served as the sole nitrogen atom source in this transformation. The diversiform functional acridines and carbazoles were comprehensively achieved through annulated diaryliodonium salts, respectively. Notably, Acridine orange (a fluorescent indicator for cell lysosomal dye) and Carprofen (a nonsteroidal anti-inflammatory drug) were efficiently established through this protocol.

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