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51690-79-0

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51690-79-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51690-79-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,6,9 and 0 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 51690-79:
(7*5)+(6*1)+(5*6)+(4*9)+(3*0)+(2*7)+(1*9)=130
130 % 10 = 0
So 51690-79-0 is a valid CAS Registry Number.

51690-79-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name [3-hydroxy-2,2-bis(hydroxymethyl)propyl] benzoate

1.2 Other means of identification

Product number -
Other names I01-8412

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:51690-79-0 SDS

51690-79-0Relevant articles and documents

Small BODIPY Probes for Combined Dual19F MRI and Fluorescence Imaging

Huynh, Anh Minh,Müller, Andreas,Kessler, Sonja M.,Henrikus, Sarah,Hoffmann, Caroline,Kiemer, Alexandra K.,Bücker, Arno,Jung, Gregor

, p. 1568 - 1575 (2016/08/20)

The combination of the two complementary imaging modalities19F magnetic resonance imaging (MRI) and fluorescence imaging (FLI) possesses high potential for biological and medical applications. Herein we report the first design, synthesis, dual detection validation, and cytotoxic testing of four promising BODIPY dyes for dual19F MRI–fluorescence detection. Using straightforward Steglich reactions, small fluorinated alcohols were easily covalently tethered to a BODIPY dye in high yields, leaving its fluorescence properties unaffected. The synthesized compounds were analyzed with various techniques to demonstrate their potential utility in dual imaging. As expected, the chemically and magnetically equivalent trifluoromethyl groups of the agents exhibited a single NMR signal. The determined longitudinal relaxation times T1and the transverse relaxation times T2, both in the lower second range, enabled the imaging of four compounds in vitro. The most auspicious dual19F MRI–fluorescence agent was also successfully imaged in a mouse post-mortem within a 9.4 T small-animal tomograph. Toxicological assays with human cells (primary HUVEC and HepG2 cell line) also indicated the possibility for animal testing.

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