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15341-08-9

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15341-08-9 Usage

Description

6-Nitropiperonyl alcohol is an organic compound that exists as a yellow powder. It is a versatile chemical with applications in both organic chemical synthesis and proteomics research.

Uses

Used in Organic Chemical Synthesis:
6-Nitropiperonyl alcohol is used as an intermediate in the synthesis of various organic compounds. Its unique chemical structure allows it to be a valuable building block for creating a wide range of molecules with different properties and functions.
Used in Proteomics Research:
In the field of proteomics, 6-Nitropiperonyl alcohol is utilized as a biochemical reagent. It plays a crucial role in the study of proteins, their structures, and functions, contributing to the advancement of our understanding of biological processes and the development of new therapeutic strategies.
Used in Pharmaceutical Industry:
6-Nitropiperonyl alcohol is also employed in the pharmaceutical industry, where it serves as a key component in the development of new drugs and drug candidates. Its versatility and reactivity make it an essential tool in the design and synthesis of novel pharmaceutical compounds.
Used in Chemical Research:
In the realm of chemical research, 6-Nitropiperonyl alcohol is used as a valuable research tool. It helps scientists explore new reaction pathways, develop innovative synthetic methods, and gain insights into the fundamental principles governing chemical reactions and interactions.
Used in Analytical Chemistry:
6-Nitropiperonyl alcohol finds application in analytical chemistry as a reagent for the detection and quantification of various compounds. Its unique chemical properties enable the development of sensitive and selective analytical methods, which are essential for accurate measurements and reliable results in various fields, including environmental monitoring, food analysis, and pharmaceutical quality control.

Check Digit Verification of cas no

The CAS Registry Mumber 15341-08-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,3,4 and 1 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 15341-08:
(7*1)+(6*5)+(5*3)+(4*4)+(3*1)+(2*0)+(1*8)=79
79 % 10 = 9
So 15341-08-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H7NO5/c10-3-5-1-7-8(14-4-13-7)2-6(5)9(11)12/h1-2,10H,3-4H2

15341-08-9 Well-known Company Product Price

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  • Alfa Aesar

  • (A18140)  6-Nitropiperonyl alcohol, 98+%   

  • 15341-08-9

  • 5g

  • 803.0CNY

  • Detail
  • Alfa Aesar

  • (A18140)  6-Nitropiperonyl alcohol, 98+%   

  • 15341-08-9

  • 25g

  • 2029.0CNY

  • Detail

15341-08-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-NITROPIPERONYL ALCOHOL

1.2 Other means of identification

Product number -
Other names (6-nitro-benzo[1,3]dioxol-5-yl)-methanol

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:15341-08-9 SDS

15341-08-9Relevant articles and documents

Tag-Free Internal RNA Labeling and Photocaging Based on mRNA Methyltransferases

Ovcharenko, Anna,Weissenboeck, Florian P.,Rentmeister, Andrea

, p. 4098 - 4103 (2021)

The mRNA modification N6-methyladenosine (m6A) is associated with multiple roles in cell function and disease. The methyltransferases METTL3-METTL14 and METTL16 act as “writers” for different target transcripts and sequence motifs. The modification is perceived by dedicated “reader” and “eraser” proteins, but not by polymerases. We report that METTL3-14 shows remarkable cosubstrate promiscuity, enabling sequence-specific internal labeling of RNA without additional guide RNAs. The transfer of ortho-nitrobenzyl and 6-nitropiperonyl groups allowed enzymatic photocaging of RNA in the consensus motif, which impaired polymerase-catalyzed primer extension in a reversible manner. METTL16 was less promiscuous but suitable for chemo-enzymatic labeling using different types of click chemistry. Since both enzymes act on distinct sequence motifs, their combination allowed orthogonal chemo-enzymatic modification of different sites in a single RNA.

Metal–Organic Framework-Encapsulated CoCu Nanoparticles for the Selective Transfer Hydrogenation of Nitrobenzaldehydes: Engineering Active Armor by the Half-Way Injection Method

Li, Yang,Li, Yu-Nong,Zheng, Jian-wei,Dong, Xiao-yun,Guo, Rong-xiu,Wang, Yi-ming,Hu, Ze-nan,Ai, Yongjian,Liang, Qionglin,Sun, Hong-bin

supporting information, p. 1080 - 1087 (2020/12/18)

A novel armor-type composite of metal–organic framework (MOF)-encapsulated CoCu nanoparticles with a Fe3O4 core (Fe3O4@SiO2-NH2-CoCu@UiO-66) has been designed and synthesized by the half-way injection method, which successfully serves as an efficient and recyclable catalyst for the selective transfer hydrogenation. In this half-way injection approach, the pre-synthetic Fe3O4@SiO2-NH2-CoCu was injected into the UiO-66 precursor solution halfway through the MOF budding period. The formed MOF armor could play a role of providing significant additional catalytic sites besides CoCu nanoparticles, protecting CoCu nanoparticles, and improving the catalyst stability, thus facilitating the selective transfer hydrogenation of nitrobenzaldehydes into corresponding nitrobenzyl alcohols in high selectivity (99 %) and conversion (99 %) rather than nitro group reduction products. Notably, this method achieves the precise assembly of a MOF-encapsulated composite, and the ingenious combination of MOF and nanoparticles exhibits excellent catalytic performance in the selective hydrogen transfer reaction, implementing a “1+1>2” strategy in catalysis.

Photocaged Carbohydrates: Versatile Tools for Controlling Gene Expression by Light

Bier, Claus,Binder, Dennis,Drobietz, Dagmar,Loeschcke, Anita,Drepper, Thomas,Jaeger, Karl-Erich,Pietruszka, J?rg

, p. 42 - 52 (2016/12/24)

The control of biological processes plays a central role in life science, especially the tight regulation of gene expression for biotechnological systems. In this context, optogenetic tools have emerged as an important instrument for controlling gene expression by light with high spatiotemporal resolution in a non-invasive way. Here, we present the syntheses and characterization of biofunctional photocaged carbohydrates, on the basis of the biologically most relevant carbohydrates glucose, galactose, rhamnose, and lactose. The single-step cleavage of these compounds allows both, to rapidly activate and temporary or permanently repress the transcription in E. coli after short UV-A light exposure. This study thus presents a versatile toolbox of photocaged carbohydrates for the light-triggered regulation and control of cellular processes useful for synthetic bio(techno)logy applications.

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