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12163-21-2

dilutetium triselenide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 12163-21-2 Structure

  • Basic information

    1. Product Name: dilutetium triselenide
    2. Synonyms: dilutetium triselenide
    3. CAS NO:12163-21-2
    4. Molecular Formula: C8H12F2O2
    5. Molecular Weight: 586.814
    6. EINECS: 235-308-6
    7. Product Categories: N/A
    8. Mol File: 12163-21-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: °Cat760mmHg
    3. Flash Point: °C
    4. Appearance: /
    5. Density: g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: dilutetium triselenide(CAS DataBase Reference)
    10. NIST Chemistry Reference: dilutetium triselenide(12163-21-2)
    11. EPA Substance Registry System: dilutetium triselenide(12163-21-2)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 12163-21-2(Hazardous Substances Data)

12163-21-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 12163-21-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,2,1,6 and 3 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 12163-21:
(7*1)+(6*2)+(5*1)+(4*6)+(3*3)+(2*2)+(1*1)=62
62 % 10 = 2
So 12163-21-2 is a valid CAS Registry Number.
InChI:InChI=1/2Lu.3Se/q2*+3;3*-2

12163-21-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name lutetium(3+),selenium(2-)

1.2 Other means of identification

Product number -
Other names lutetium selenide(2:3)

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:12163-21-2 SDS

12163-21-2Downstream Products

12163-21-2Relevant articles and documents

TRICYCLIC COMPOUND SERVING AS IMMUNOMODULATOR

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Paragraph 0298-0299, (2019/01/04)

Provided are compounds of formula I and formula II or pharmaceutically acceptable salts of the compounds and pharmaceutical compositions thereof. The compounds of formula I and formula II or the pharmaceutically acceptable salts of the compounds provide indole 2,3-dioxygenase (IDO) inhibitory activity and are capable of treating IDO-mediated immunosuppressive diseases, such as infectious diseases or cancer.

CYCLOALKYL METHOXYBENZYL PHENYL PYRAN DERIVATIVES AS SODIUM DEPENDENT GLUCOSE CO TRANSPORTER (SGLT2) INHIBITORS

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Page/Page column 44-45, (2012/03/26)

The invention relates to the cycloalkyl methoxybenzyl phenyl pyran derivatives as Sodium dependent glucose co transporter (SGLT) inhibitors, particularly SGLT2 and method of treating diseases, conditions and/or disorders inhibited by SGLT2 with them, and processes for preparing them.

Fluorinated carbocylic compounds

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, (2008/06/13)

Fluoro-substituted carbocyclic compounds are prepared by (A) reacting hydrogen fluoride with a chloro-cyclohexenyl compound of the formula STR1 where R1 and R2 are independently selected from the group consisting of --H, --CH2 OH, --COF, --COCl, --CF3, --CN, STR2 and --CH2 R, where R is --H or alkyl of 1-4 carbon atoms, to form a gem-dihalocyclohexane compound of the formula STR3 where X is chlorine and R1 and R2 are as defined above, (B) dehydrohalogenating the gem-dihalocyclohexane compound in the vapor phase to form a fluoro-cyclohexenyl compound of the formula STR4 (C) contacting the fluoro-cyclohexenyl compound, in the vapor phase, with a dehydrogenation catalyst to form a fluoro-substituted aromatic compound of the formula STR5

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