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Methylthiazol-2-ylcarbaMic acid tert-butyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 479198-74-8 Structure
  • Basic information

    1. Product Name: Methylthiazol-2-ylcarbaMic acid tert-butyl ester
    2. Synonyms: Methylthiazol-2-ylcarbaMic acid tert-butyl ester
    3. CAS NO:479198-74-8
    4. Molecular Formula: C9H14N2O2S
    5. Molecular Weight: 214.28466
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 479198-74-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 268.2±23.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.192±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 3.68±0.10(Predicted)
    10. CAS DataBase Reference: Methylthiazol-2-ylcarbaMic acid tert-butyl ester(CAS DataBase Reference)
    11. NIST Chemistry Reference: Methylthiazol-2-ylcarbaMic acid tert-butyl ester(479198-74-8)
    12. EPA Substance Registry System: Methylthiazol-2-ylcarbaMic acid tert-butyl ester(479198-74-8)
  • 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: 479198-74-8(Hazardous Substances Data)

479198-74-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 479198-74-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,9,1,9 and 8 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 479198-74:
(8*4)+(7*7)+(6*9)+(5*1)+(4*9)+(3*8)+(2*7)+(1*4)=218
218 % 10 = 8
So 479198-74-8 is a valid CAS Registry Number.

479198-74-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl N-methyl-N-(1,3-thiazol-2-yl)carbamate

1.2 Other means of identification

Product number -
Other names Methylthiazol-2-ylcarbamic acid 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:479198-74-8 SDS

479198-74-8Relevant articles and documents

INHIBITORS OF HEAT SHOCK FACTORS AND USES THEREOF

-

, (2018/04/13)

The present disclosure relates to a class of mammalian heat shock factor (HSF) inhibitors, to pharmaceutical compositions comprising these inhibitors as well as to methods for using the inhibitors. The inhibitors inhibit stress-induced expression from heat shock gene promoters. Furthermore, the inhibitors are cytotoxic to a variety of human cancer cells types.

BENZOXAZOLE DERIVATIVES

-

Page/Page column 60, (2009/10/01)

It is intended to provide a benzoxazole derivative or a pharmaceutically acceptable salt or solvate thereof which is useful in the early diagnosis of a conformation disease; a composition or a kit containing the same for diagnosing a conformation disease; a medical composition for ttreating and/or preventing a conformation disease; and so on.

A short and highly stereoselective synthesis of α-(2-aminothiazolyl)-C-nucleosides

Navarre, Jean-Michel,Guianvarc'h, Dominique,Farese-Di Giorgio, Audrey,Condom, Roger,Benhida, Rachid

, p. 2199 - 2202 (2007/10/03)

A short route to novel α-(2-aminothiazolyl)-C-nucleosides has been developed. The key step was the high diastereoselective reduction of the hemiacetal intermediates using L-Selectride, which afforded the corresponding R-diols in quantitative yields. These diols were converted, after C4-C1 ring closure and protecting groups cleavage, to their corresponding free α-C-nucleosides.

Synthesis, incorporation into triplex-forming oligonucleotide, and binding properties of a novel 2'-deoxy-C-nucleoside featuring a 6-(thiazolyl-5)benzimidazole nucleobase.

Guianvarc'h, Dominique,Fourrey, Jean-Louis,Maurisse, Rosalie,Sun, Jian-Sheng,Benhida, Rachid

, p. 4209 - 4212 (2007/10/03)

[reaction: see text] 6-(Thiazolyl-5)benzimidazole (B(t)()) was designed as a novel nucleobase for the specific recognition of an inverted A.T base pair in a triple helix motif. It was successfully incorporated into an 18-mer triplex-forming oligonucleotid

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