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192635-89-5

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192635-89-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 192635-89-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,2,6,3 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 192635-89:
(8*1)+(7*9)+(6*2)+(5*6)+(4*3)+(3*5)+(2*8)+(1*9)=165
165 % 10 = 5
So 192635-89-5 is a valid CAS Registry Number.

192635-89-5SDS

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 phenylmethyl 2-(1,4,7,10-Tetraaza-4,7,10-tris(((tert-butyl)oxycarbonyl)methyl)cyclododecyl)-acetate

1.2 Other means of identification

Product number -
Other names N-(carbobenzoxymethyl)-1,4,7,10-tetraazacyclododecane-N',N'',N'''-triacetic acid tri-tert-butyl ester

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:192635-89-5 SDS

192635-89-5Relevant articles and documents

Multivalent Siderophore–DOTAM Conjugates as Theranostics for Imaging and Treatment of Bacterial Infections

Ferreira, Kevin,Hu, Hai-Yu,Fetz, Verena,Prochnow, Hans,Rais, Bushra,Müller, Peter P.,Br?nstrup, Mark

, p. 8272 - 8276 (2017)

There is a strong need to better diagnose infections at deep body sites through noninvasive molecular imaging methods. Herein, we describe the synthesis and characterization of probes based on siderophore conjugates with catechol moieties and a central DO

NIR/PET bimodal contrast agent, and preparation method and application thereof

-

, (2021/07/24)

The invention discloses a near infrared and positron emission computed tomography (NIR)/positron emission tomography (PET) bimodal contrast agent, and a preparation method and application thereof. The NIR/PET bimodal contrast agent is obtained by taking an optimized indocyanine green derivative as a carrier and connecting a PET signal molecule. The contrast agent can be used for near-infrared imaging and has PET imaging capability; and meanwhile, the contrast agent is good in water solubility and low in toxicity, near-infrared and PET images verify each other, diagnosis information is enriched, and the contrast agent has the potential of becoming a novel tumor contrast agent.

Time-Resolved Terbium-Based Probe for the Detection of Zinc(II) Ions: Investigation of the Formation of a Luminescent Ternary Complex

Winnett, Matthew R.,Mini, Parvathy,Grace, Michael R.,Tuck, Kellie L.

supporting information, p. 118 - 127 (2019/09/30)

Because of their unique photochemical and photophysical properties, luminescent lanthanide-based complexes have long captivated chemists. In recent years, the number of reports of luminescent lanthanide complex-based probes for monitoring of biological an

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