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145190-98-3

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145190-98-3 Usage

Chemical Properties

Pale Yellow Oil

Uses

3-Tri-N-butylstannyl-phenylisothiocyanate is a compound used potentially for the radioiodination of monoclonal antibodies. Used in Antibody labelling.

Check Digit Verification of cas no

The CAS Registry Mumber 145190-98-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,1,9 and 0 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 145190-98:
(8*1)+(7*4)+(6*5)+(5*1)+(4*9)+(3*0)+(2*9)+(1*8)=133
133 % 10 = 3
So 145190-98-3 is a valid CAS Registry Number.

145190-98-3SDS

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-Tri-N-butylstannyl-phenylisothiocyanate

1.2 Other means of identification

Product number -
Other names tributyl-(3-isothiocyanatophenyl)stannane

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:145190-98-3 SDS

145190-98-3Downstream Products

145190-98-3Relevant articles and documents

Integrated Synthesis Using Isothiocyanate-Substituted Aryllithiums by Flow Chemistry

Lee, Hyune-Jea,Torii, Daiki,Jeon, Yongju,Yoshida, Jun-Ichi,Kim, Heejin

, p. 1899 - 1902 (2020)

The isothiocyanate (NCS) group is an attractive functional group in the field of organic and pharmaceutical chemistry. It can be transformed into other heteroatomic functional groups. It usually acts as the inductive group of biological activity and has also been traditionally used as the fluorescent-labeling reagent. However, it is not compatible with strong bases. When the NCS group is at para position in halobenzenes, it generally undergoes nucleophilic additions upon reaction with strong bases. To the best of our knowledge, there is currently no general methodology for the formation and reactions of NCS-functionalized aryllithiums for meta and para substituents. Herein, we report the continuous-flow generation of NCS-substituted aryllithiums from the corresponding haloarenes via a selective halogen-lithium exchange reaction and its reaction with various electrophiles to yield NCS-containing products. We also achieved an integrated synthesis through sequential reactions of the NCS-containing compounds with additional nucleophiles using the continuous-flow reactors.

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