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1-(2-Nitrophenyl)-1,2-ethanediol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51673-59-7

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51673-59-7 Usage

Synthesis Reference(s)

Canadian Journal of Chemistry, 61, p. 400, 1983 DOI: 10.1139/v83-072

Check Digit Verification of cas no

The CAS Registry Mumber 51673-59-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,6,7 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 51673-59:
(7*5)+(6*1)+(5*6)+(4*7)+(3*3)+(2*5)+(1*9)=127
127 % 10 = 7
So 51673-59-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H9NO4/c10-5-8(11)6-3-1-2-4-7(6)9(12)13/h1-4,8,10-11H,5H2

51673-59-7 Well-known Company Product Price

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  • Aldrich

  • (274526)  1-(2-Nitrophenyl)-1,2-ethanediol  98%

  • 51673-59-7

  • 274526-1G

  • 2,177.37CNY

  • Detail
  • Aldrich

  • (274526)  1-(2-Nitrophenyl)-1,2-ethanediol  98%

  • 51673-59-7

  • 274526-5G

  • 7,218.90CNY

  • Detail

51673-59-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-Nitrophenyl)-1,2-ethanediol

1.2 Other means of identification

Product number -
Other names 2-NITROSTYRENE GLYCOL

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:51673-59-7 SDS

51673-59-7Relevant academic research and scientific papers

Photoregulation of Gene Expression with Amantadine-Modified Caged siRNAs through Host–Guest Interactions

Zhang, Jinhao,Jing, Nannan,Fan, Xinli,Tang, Xinjing

, p. 14002 - 14010 (2020/10/02)

RNA interference is an essential and powerful tool for targeting and verifying specific gene functions. Conditional control of small interfering RNA (siRNA) activity, especially using light activation, is a potential method for regulating target gene expr

A photoactivatable microRNA probe for identification of microRNA targets and light-controlled suppression of microRNA target expression

Chen, Lei,Li, Jinbo,Sun, Yu.,Zhang, Yan

, p. 627 - 630 (2020/01/29)

Here, we report a novel dual-functional microRNA (miRNA) probe, PA-miRNA, for miRNA target identification and light control of miRNA target expression. PA-miRNA is a miRNA mimic with a 3′-biotin tag linked via a photo-cleavable linker. Using PA-miR-34a, i

Photochemical regulation of gene expression using caged siRNAs with single terminal Vitamin E modification

Ji, Yuzhuo,Yang, Jiali,Wu, Li,Yu, Lijia,Tang, Xinjing

, p. 2152 - 2156 (2016/02/18)

Caged siRNAs with a single photolabile linker and/or vitamin E (vitE) modification at the 5′ terminal were rationally designed and synthesized. These virtually inactive caged siRNAs were successfully used to photoregulate both firefly luciferase and GFP g

A rapid 1,2-dihydroxylation of alkenes using a lipase and hydrogen peroxide under microwave conditions

Sarma, Kuladip,Borthakur, Naleen,Goswami, Amrit

, p. 6776 - 6778 (2008/02/13)

The combined advantages of using an enzyme immobilized lipase from Pseudomonas sp [PSLG6], hydrogen peroxide, ethyl acetate and microwave irradiation for the dihydroxylation of olefins are reported.

Photocleavable circular oligonucleotides

-

, (2008/06/13)

The photocleavable cyclic oligonucleotide according to the invention is the one that possesses a base sequence having the hybridization ability toward DNA or RNA to targeted, and is further provided with the structure cyclized by a photocleavable group. Accordingly, the photocleavable cyclic oligonucleotide according to the invention, after having been introduced in vivo, is hardly susceptible to the nuclease decomposition reaction owing to its cyclic structure and thus it is capable of diffusing toward the predetermined sites in vivo with sufficient time. Moreover, by being irradiated with the light at an appropriate wavelength after a predetermined period of time, the photocleavable group as described above is cleaved photochemically, thus cutting the predetermined bond. This permits the oligonucleotide that was cyclic to be a linear oligonucleotide which expresses the function of an antisense oligonucleotide.

Behavior modifying compounds

-

, (2008/06/13)

Derivatives of carbonyl-group containing behavior modifying compounds, in which said carbonyl group has been converted to a photolabile group which regenerates the carbonyl group on exposure to radiation, are of value in various methods for the control of

Antibacterial Benzisoxazolones. An Unusual Rearrangement Product from o-Nitrostyrene Oxide en Route to the Photolabile Carbonyl Protecting Group (o-Nitrophenyl)ethylene Glycol

Wierenga, Wendell,Harrison, Allen W.,Evans, Bruce R.,Chidester, Connie G.

, p. 438 - 442 (2007/10/02)

In the process of synthesizing the known, photolabile protecting group (o-nitrophenyl)ethylene glycol, we uncovered an acid-mediated rearrangement of o-nitrostyrene oxide to 1-(hydroxymethyl)-2,1-benzisoxazol-3(1H)-one.The structure was ascertained by IR, UV, 1H NMR, 13C NMR, MS, and X-ray crystallography.Also the benzisoxazolone was prepared by independent synthesis from an o-nitrobenzoate.Another novel transformation uncovered was the conversion of o-nitrostyrene oxide to 2-(o-nitrophenyl)ethanol with use of potassium hydroxide and 18-crown-6.Similiar chemistry was insignificant with p-nitrostyrene oxide.The benzisoxazolone exhibited antibacterial and antileukemic activity (in vitro).

o-Nitrophenylethylene glycol as photoremovable protective group for aldehydes and ketones: syntheses, scope, and limitations

Gravel, D.,Herbert, J.,Thoraval, D.

, p. 400 - 410 (2007/10/02)

The preparation of o-nitophenylethylene glycol is described along with its application as a photolabile protective group for aldehydes and ketones.Formation of the acetals and ketals is achieved in good to high yields in the usual manner and deprotection is carried out in fair to high yield, by photolysis at 350 nm in an inert solvent such as benzene.Because of the particular nature of the present protective group, its stability to basic and acidic conditions has been examined and is reported to complete the scope and limitations aspect.From a mechanistic point of view, the isolation and characterisation of o-nitroso-α-hydroxyacetophenone as the spent reagent demonstrates a mechanistic link with the known o-nitrobenzaeldehyde to o-nitrobenzoic acid photorearrangement.

Substituted dioxolanes and photosensitive and degradable polymers useful in imaging

-

, (2008/06/13)

Substituted dioxolanes are provided having the formula STR1 wherein R1 and R2 are H or a phenyl group substituted with up to 5 substituents of lower alkyl or nitro, with the proviso that at least one of F1 and R2/sup

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