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4-Pentene-1,2-diol, 1,2-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56072-16-3

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56072-16-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56072-16-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,0,7 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 56072-16:
(7*5)+(6*6)+(5*0)+(4*7)+(3*2)+(2*1)+(1*6)=113
113 % 10 = 3
So 56072-16-3 is a valid CAS Registry Number.

56072-16-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-diphenylpent-4-ene-1,2-diol

1.2 Other means of identification

Product number -
Other names 4-Pentene-1,2-diol,1,2-diphenyl

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:56072-16-3 SDS

56072-16-3Relevant academic research and scientific papers

Ready Access to Densely Substituted Furans Using Tsuji-Wacker-Type Cyclization

Masal, Dattatraya P.,Choudhury, Rahul,Singh, Aman,Reddy, D. Srinivasa

, p. 556 - 568 (2022/01/14)

A competent method for the construction of highly substituted furans catalyzed by Pd(II) and Cu(II) chloride has been developed. The method provides easy access to di-, tri-, and tetrasubstituted furans from corresponding diols with relatively mild condit

Indirect Tertiary Alcohol Enantiocontrol by Acylative Organocatalytic Kinetic Resolution

Amalian, Jean-Arthur,Bressy, Cyril,Charles, Laurence,Desrues, Titouan,Liu, Xueyang,Monnier, Valérie,Pons, Jean-Marc,Quintard, Adrien

supporting information, p. 4332 - 4336 (2021/06/27)

The stereocontrol of tertiary alcohols represents a recurrent challenge in organic synthesis. In the present paper, we describe a simple, efficient, and indirect method to enantioselectively prepare tertiary alcohols through a chiral isothiourea catalyzed

Zinc-Mediated Efficient and Selective Reduction of Carbonyl Compounds

Mandal, Tirtha,Jana, Snehasish,Dash, Jyotirmayee

, p. 4972 - 4983 (2017/09/13)

We herein describe for the first time that an optimized combination of Zn and NH4Cl can be used for the selective reduction of aldehydes and ketones to the corresponding alcohols. The aldehyde and keto groups are selectively reduced in the presence of azide, cyano, epoxy, ester, and carbon–carbon double-bond functional groups. A broad functional-group compatibility, chemoselective reduction of aldehydes in the presence of ketones, and selective reduction of isatins at the C3 carbonyl group are the highlights of the present method.

2, 3-Diaryl-5-ethylsulfanylmethyltetrahydrofurans as a new class of COX-2 inhibitors and cytotoxic agents

Singh, Palwinder,Mittal, Anu,Kaur, Satwinderjeet,Holzer, Wolfgang,Kumar, Subodh

scheme or table, p. 2706 - 2712 (2009/02/03)

2,3-Diaryl-5-ethylsulfanylmethyltetrahydrofuran-3-ols were designed and synthesized by the allylations of benzoins followed by iodocyclization and nucleophilic replacement reactions with ethanthiol. These molecules exhibit IC50 for COX-2 at 50 over all the 59 human tumor cell lines at μ M concentration. The Royal Society of Chemistry.

2,3,5-Substituted tetrahydrofurans: COX-2 inhibitory activities of 5-hydroxymethyl-/carboxyl-2,3-diaryl-tetrahydro-furan-3-ols

Singh, Palwinder,Mittal, Anu,Kaur, Satwinderjeet,Kumar, Subodh

body text, p. 2792 - 2799 (2009/04/05)

5-Hydroxymethyl-/carboxyl-2,3-diaryl-tetrahydro-furan-3-ols have been investigated for their COX-1 and COX-2 inhibitory activities. Compounds 17, 18 and 20 have been identified as showing appreciable COX-2 inhibition and selectivity. The group present at

Regio- and stereochemical aspects in the synthesis of homoallylic alcohols from benzoins and their iodocyclisation to 2,3-diphenyltetrahydrofurans

Kumar, Subodh,Kaur, Pervinder,Mittal, Anu,Singh, Palwinder

, p. 4018 - 4026 (2007/10/03)

Indium mediated allylation, crotylation and cinnamylation of benzoins and its substituted derivatives in THF-H2O (2/1) provide a range of homoallylic alcohols. In general, the benzoins undergo allylation and crotylation in a sluggish manner com

5-Substituted-2,3-diphenyltetrahydrofurans: A new class of moderately selective COX-2 inhibitors

Singh, Palwinder,Mittal, Anu,Kaur, Satwinderjit,Kumar, Subodh

, p. 7910 - 7916 (2007/10/03)

The nature of C-5 substituent and the configuration at C-5 carbon of 2,3-diphenyltetrahydrofurans, with chiral centres at C-2, C-3 and C-5, show a remarkable influence on their COX-2 inhibition and selectivity. Out of the eight compounds investigated here

Barbier coupling in water: SnCl2-mediated and Co(acac) 2-catalyzed allylation of carbonyls

Chaudhuri, Mihir K.,Dehury, Sanjay K.,Hussain, Sahid

, p. 6247 - 6251 (2007/10/03)

Co(acac)2·2H2O efficiently catalyzes SnCl 2-mediated Barbier coupling in water between carbonyls, including aromatic, aliphatic and α,β-unsaturated aldehydes, ketones, sugars and allyl bromide to afford the corresponding h

Ceric(IV) ammonium nitrate: A novel reagent for the synthesis of homoallyl alcohols

Yadav,Reddy,Krishna,Sadasiv,Chary, Ch. Janardhana

, p. 248 - 249 (2007/10/03)

A rapid and highly efficient method has been developed for the allylation of aldehydes with allyltributylstannane using a catalytic amount of eerie ammonium nitrate in acetonitrile under mild and neutral conditions to afford the corresponding homoallyl al

Remarkable enhancement of Lewis acidity of chlorosilane by the combined use of indium(III) chloride

Onishi, Yoshiyuki,Ito, Takeshi,Yasuda, Makoto,Baba, Akio

, p. 8227 - 8235 (2007/10/03)

A combination of InCl3 and R3SiCl provided a strong Lewis acid catalyst for such reactions as allylation, hydrosilation and Friedel-Crafts alkylation. Especially, catalytic Sakurai-Hosomi-type allylation was accomplished with high yield and selectivity. The silicon atom is assumed to be the acidic center of the combined system, and the catalytic activity largely depends on the substituents on the silicon center.

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