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66224-70-2

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66224-70-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66224-70-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,2,2 and 4 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 66224-70:
(7*6)+(6*6)+(5*2)+(4*2)+(3*4)+(2*7)+(1*0)=122
122 % 10 = 2
So 66224-70-2 is a valid CAS Registry Number.

66224-70-2SDS

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-trimethylsilylpropynoic acid chloride

1.2 Other means of identification

Product number -
Other names 3-trimethylsilyl-2-propynoyl chloride

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:66224-70-2 SDS

66224-70-2Relevant articles and documents

Synthesis of unstable carbides Ag2C2n (n = 3, 4) and characterization via crystallographic analysis of their double salts with silver(I) trifluoroacetate

Hau, Sam C. K.,Mak, Thomas C. W.

, p. 902 - 905 (2014)

Two new silver(I) carbides, Ag2C6 and Ag 2C8, have been synthesized, and single-crystal X-ray analysis of their crystalline silver(I) trifluoroacetate complexes, Ag 2C6·8AgCF3CO2·6H 2O, 4(Ag2C6)·16AgCF3CO 2·14.5DMSO, and 2.5(Ag2C8) ·10AgCF3CO2·10DMSO, provides detailed information on the influence of ligand disposition and orientation of the all-carbon anionic ligands in the construction of multidimensional supramolecular structures, which are consolidated by argentophilic and weak inter-/intramolecular interactions.

One-pot synthesis of 3-(trimethylsilyl)propynamides

Medvedeva,Andreev,Safronova

, p. 1466 - 1470 (2010)

A highly efficient one-pot procedure was developed for the synthesis of 3-trimethylsilylpropynamides by acylation of amines with trimethylsilylpropynoyl chloride generated in situ. Selective N-acylation and N,O-bis-acylation of -amino alcohols with format

COMPOUNDS AND METHODS OF USE

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Page/Page column 195; 197, (2022/03/09)

Disclosed are heterocyclic compounds or their pharmaceutically acceptable salts with ferroptosis-inducing activity, Those compounds or their pharmaceutically acceptable salts can be used to treat cancer.

CATHEPSIN C INHIBITORS

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Paragraph 0171-0174, (2020/01/24)

Disclosed are compounds, pharmaceutical compositions used for inhibiting cathepsin C without inhibiting epidermal growth factor receptor (EGFR).

INHIBITORS OF RAC1 AND USES THEREOF FOR TREATING CANCERS

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Paragraph 0113-0115, (2019/01/04)

The present invention concerns a compound having the following formula (I): wherein: - A is in particular -N(R'a)-C(=O)-R, R'a being H or a (C1-C6)alkyl group, and R being preferably a group having the following formula (II): - X is in particular chosen from the group consisting of: -SO2-N(R'b)-, R'b being H or a (C1-C6)alkyl group, -N(R"b)-SO2-, R"b being H or a (C1-C6)alkyl group, -CO-NH-, and -NH-CO-, for use for the treatment of cancers, such as metastatic cancers.

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