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3-hydroxyphenyl-3H-diazirine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

80863-10-1

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80863-10-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80863-10-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,8,6 and 3 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 80863-10:
(7*8)+(6*0)+(5*8)+(4*6)+(3*3)+(2*1)+(1*0)=131
131 % 10 = 1
So 80863-10-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H6N2O/c10-6-3-1-2-5(4-6)7-8-9-7/h1-4,7,10H

80863-10-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(3H-diazirin-3-yl)phenol

1.2 Other means of identification

Product number -
Other names MHPDA

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:80863-10-1 SDS

80863-10-1Relevant academic research and scientific papers

Sites of Photolytic Intermolecular Cross-Linking between Fatty Acyl Chains in Phospholipids Carrying a Photoactivable Carbene Precursor

Radhakrishnan, Ramachandran,Costello, Catherine E.,Khorana, H. Gobind

, p. 3990 - 3997 (2007/10/02)

A number of sn-glycero-3-phosphorylcholines containing the photosensitive ω-undecanoyl group in the sn-2 position and a dideuterated palmitic or stearic acid with both deuteriums on specific carbon atoms along the hydrocarbon chain in the sn-1 position were synthesized.Photolysis of either sonicated vesicles or multilamellar dispersions prepared from these synthetic phospholipids gave extensive intermolecularly cross-linked products.The distribution of the sites of cross-linking was determined by an analysis of cross-linked dimeric fatty esters by using low-resolution electron impact mass spectrometry.The predominance of the benzylic cleavage with a γ-hydrogen abstraction in the mass spectra of these diesters rendered such a quantitation relatively easy.Mass spectral analysis showed that there is a broad distribution in the cross-linking positions along the deuterated sn-1 chain, with the amount of cross-linking increasing toward the hydrophobic core of the bilayer.These results are in agreement with the conformational mobility of the fatty acyl chains and the localization of the photosensitive diazirinophenoxy group in the middle of the bilayer.

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