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Benzenemethanol, 4-(azidomethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 439691-96-0 Structure
  • Basic information

    1. Product Name: Benzenemethanol, 4-(azidomethyl)-
    2. Synonyms:
    3. CAS NO:439691-96-0
    4. Molecular Formula: C8H9N3O
    5. Molecular Weight: 163.179
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 439691-96-0.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: Benzenemethanol, 4-(azidomethyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzenemethanol, 4-(azidomethyl)-(439691-96-0)
    11. EPA Substance Registry System: Benzenemethanol, 4-(azidomethyl)-(439691-96-0)
  • 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: 439691-96-0(Hazardous Substances Data)

439691-96-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 439691-96-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,9,6,9 and 1 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 439691-96:
(8*4)+(7*3)+(6*9)+(5*6)+(4*9)+(3*1)+(2*9)+(1*6)=200
200 % 10 = 0
So 439691-96-0 is a valid CAS Registry Number.

439691-96-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-(azidomethyl)phenyl)methanol

1.2 Other means of identification

Product number -
Other names [4-(azidomethyl)phenyl]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:439691-96-0 SDS

439691-96-0Relevant articles and documents

Sustainable organophosphorus-catalysed Staudinger reduction

Lenstra, Danny C.,Lenting, Peter E.,Mecinovi?, Jasmin

, p. 4418 - 4422 (2018/10/17)

A highly efficient and sustainable catalytic Staudinger reduction for the conversion of organic azides to amines in excellent yields has been developed. The reaction displays excellent functional group tolerance to functionalities that are otherwise prone to reduction, such as sulfones, esters, amides, ketones, nitriles, alkenes, and benzyl ethers. The green nature of the reaction is exemplified by the use of PMHS, CPME, and a lack of column chromatography.

GLUCOSE SENSOR MOLECULE

-

Page/Page column 17, (2012/07/28)

The present invention provides a glucose sensor having a glucose receptor containing a binding site of formula (I): wherein X, n, m and R1 are defined herein. Also provided is a glucose sensor molecule for use in such a glucose sensor, the glucose sensor molecule containing the binding site of formula (I). The binding site has been found to have particularly good selectivity for glucose.

N-((6-AMINO-PYRIDIN-3-YL)METHYL)-HETEROARYL-CARBOXAMIDES

-

Page/Page column 70, (2012/02/15)

The invention relates to compound of the formula I in which the substituents are as defined in the specification; in free form or in salt form; to its preparation, to its use as medicament and to medicaments comprising it.

One- and two-photon live cell imaging using a mutant SNAP-Tag protein and its FRET substrate pairs

Zhang, Chong-Jing,Li, Lin,Chen, Grace Y. J.,Xu, Qing-Hua,Yao, Shao Q.

supporting information; experimental part, p. 4160 - 4163 (2011/10/09)

A small molecule-assisted protein labeling strategy based on a mutant SNAP-Tag (mSNAP) and its FRET substrate pairs has been developed. Both one- and two-photon fluorescence microscopic experiments were successfully demonstrated in living cells.

Derivatives of squaric acid with anti-proliferative activity

-

Page/Page column 26, (2008/12/08)

The present invention provides derivatives of squaric acid, in particular derivatives of 3,4-diamino-cyclobut-3-ene-1,2-dione and tautomers and isomers thereof, as a single stereoisomer or a mixture of stereoisomers, or as a pharmaceutically acceptable sa

Derivatives of squaric acid with anti-proliferative activity

-

Page/Page column 37, (2008/06/13)

The present invention provides derivatives of squaric acid, in particular derivatives of 3,4-diamino-cyclobut-3-ene-1,2-dione and tautomers thereof, as a single stereoisomer or a mixture of stereoisomers, or as a pharmaceutically acceptable salt thereof.

Synthesis of new AB2 monomers for polymerization to hyperbranched polymers by 1,3-dipolar cycloaddition

Smet, Mario,Metten, Kris,Dehaen, Wim

, p. 1097 - 1108 (2007/10/03)

A number of AB2 monomers containing either one azide and two acetylene functions or vice versa have been prepared. Upon polymerization, these compounds were found to give rise to hyperbranched oligomers as detected by NMR spectroscopy. However, the formation of high-molecular-weight polymers could not be proven by GPC analysis. Crosslinking was found to be a major drawback of this approach to hyperbranched polymers. Two examples of the interesting situation in which the polymerization already starts during the introduction of the polymerizable group are described.

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