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Benzoic acid, 4-nitro-, 2,2-dimethylhydrazide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 14908-42-0 Structure
  • Basic information

    1. Product Name: Benzoic acid, 4-nitro-, 2,2-dimethylhydrazide
    2. Synonyms:
    3. CAS NO:14908-42-0
    4. Molecular Formula: C9H11N3O3
    5. Molecular Weight: 209.205
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 14908-42-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Benzoic acid, 4-nitro-, 2,2-dimethylhydrazide(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzoic acid, 4-nitro-, 2,2-dimethylhydrazide(14908-42-0)
    11. EPA Substance Registry System: Benzoic acid, 4-nitro-, 2,2-dimethylhydrazide(14908-42-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 14908-42-0(Hazardous Substances Data)

14908-42-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14908-42-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,9,0 and 8 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 14908-42:
(7*1)+(6*4)+(5*9)+(4*0)+(3*8)+(2*4)+(1*2)=110
110 % 10 = 0
So 14908-42-0 is a valid CAS Registry Number.

14908-42-0SDS

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 4-nitrobenzoic 1,1-dimethylhydrazide

1.2 Other means of identification

Product number -
Other names 2-(4-Nitro-benzoyl)-1.1-dimethyl-hydrazin

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:14908-42-0 SDS

14908-42-0Relevant articles and documents

N-Ammonium Ylide Mediators for Electrochemical C-H Oxidation

Saito, Masato,Kawamata, Yu,Meanwell, Michael,Navratil, Rafael,Chiodi, Debora,Carlson, Ethan,Hu, Pengfei,Chen, Longrui,Udyavara, Sagar,Kingston, Cian,Tanwar, Mayank,Tyagi, Sameer,McKillican, Bruce P.,Gichinga, Moses G.,Schmidt, Michael A.,Eastgate, Martin D.,Lamberto, Massimiliano,He, Chi,Tang, Tianhua,Malapit, Christian A.,Sigman, Matthew S.,Minteer, Shelley D.,Neurock, Matthew,Baran, Phil S.

supporting information, p. 7859 - 7867 (2021/05/26)

The site-specific oxidation of strong C(sp3)-H bonds is of uncontested utility in organic synthesis. From simplifying access to metabolites and late-stage diversification of lead compounds to truncating retrosynthetic plans, there is a growing need for new reagents and methods for achieving such a transformation in both academic and industrial circles. One main drawback of current chemical reagents is the lack of diversity with regard to structure and reactivity that prevents a combinatorial approach for rapid screening to be employed. In that regard, directed evolution still holds the greatest promise for achieving complex C-H oxidations in a variety of complex settings. Herein we present a rationally designed platform that provides a step toward this challenge using N-ammonium ylides as electrochemically driven oxidants for site-specific, chemoselective C(sp3)-H oxidation. By taking a first-principles approach guided by computation, these new mediators were identified and rapidly expanded into a library using ubiquitous building blocks and trivial synthesis techniques. The ylide-based approach to C-H oxidation exhibits tunable selectivity that is often exclusive to this class of oxidants and can be applied to real-world problems in the agricultural and pharmaceutical sectors.

PREPARATION OF HYDRAZIDES USING SILICON TETRACHLORIDE AS COUPLING AGENT

Kornet, Milton J.,Tita, Terence T.,Thio, Alan P.

, p. 1261 - 1274 (2007/10/02)

Silicon tetrachloride proved to be an effective reagent for the preparation of hydrazides from carboxylic acids.Yields were comparable to those obtained via N,N'-dicyclohexylcarbodiimide (DCC) and the procedure was used to synthesize some hydrazides which are difficult to obtain otherwise.

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