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1,3-Bis(trimethylsilyl)urea. is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 127290-39-5 Structure
  • Basic information

    1. Product Name: 1,3-Bis(trimethylsilyl)urea.
    2. Synonyms:
    3. CAS NO:127290-39-5
    4. Molecular Formula: C7H20N2OSi2
    5. Molecular Weight: 204.42
    6. EINECS: 242-177-9
    7. Product Categories: N/A
    8. Mol File: 127290-39-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1,3-Bis(trimethylsilyl)urea.(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,3-Bis(trimethylsilyl)urea.(127290-39-5)
    11. EPA Substance Registry System: 1,3-Bis(trimethylsilyl)urea.(127290-39-5)
  • 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: 127290-39-5(Hazardous Substances Data)

127290-39-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 127290-39-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,2,9 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 127290-39:
(8*1)+(7*2)+(6*7)+(5*2)+(4*9)+(3*0)+(2*3)+(1*9)=125
125 % 10 = 5
So 127290-39-5 is a valid CAS Registry Number.

127290-39-5Relevant articles and documents

Silica Metal Oxide Vesicles Catalyze Comprehensive Prebiotic Chemistry

Mattia Bizzarri, Bruno,Botta, Lorenzo,Pérez-Valverde, Maritza Iveth,Saladino, Raffaele,Di Mauro, Ernesto,García-Ruiz, Juan Manuel

, p. 8126 - 8132 (2018/05/29)

It has recently been demonstrated that mineral self-assembled structures catalyzing prebiotic chemical reactions may form in natural waters derived from serpentinization, a geological process widespread in the early stages of Earth-like planets. We have s

Synthesis and degradation of nucleic acid components by formamide and iron sulfur minerals

Saladino, Raffaele,Neri, Veronica,Crestini, Claudia,Costanzo, Giovanna,Graciotti, Michele,Di Mauro, Ernesto

experimental part, p. 15512 - 15518 (2009/03/12)

We describe the one-pot synthesis of a large panel of nucleic bases and related compounds from formamide in the presence of iron sulfur and iron-copper sulfur minerals as catalysts. The major products observed are purine, 1H-pyrimidinone, isocytosine, adenine, 2-aminopurine, carbodiimide, urea, and oxalic acid. Isocytosine and 2-aminopurine may recognize natural nucleobases by Watson-Crick and reverse Watson-Crick interactions, thus suggesting novel scenarios for the origin of primordial nucleic acids. Since the major problem in the origin of informational polymers is the instability of their precursors, we also investigate the effects of iron sulfur and iron-copper sulfur minerals on the stability of ribooligonucleotides in formamide and in water. All of the iron sulfur and iron-copper sulfur minerals stimulated degradation of RNA. The relevance of these findings with respect to the origin of informational polymers is discussed.

Catalyst for use in production of epoxide, method for producing the catalyst, and method for producing epoxide

-

, (2008/06/13)

To provide an epoxide-production-use catalyst that is suitably used for producing an epoxide by partial oxidation of an unsaturated hydrocarbon, a catalyst in accordance with the present invention is obtained by fixing gold fine particles to a carrier containing an oxide containing at least one of titanium and zirconium, and has an acid quantity of not more than 0.1 mmol/g determined by the NH3-TPD method. Such a catalyst for epoxide producing use can be produced by, for instance, fixing gold fine particles to a carrier having an acid quantity of not more than 0.15 mmol/g. The catalyst for epoxide producing use arranged as above is preferably used as a catalyst in partial oxidation of an unsaturated hydrocarbon to produce a corresponding epoxide.

Carbacephalosporin compound, their preparation and use

-

, (2008/06/13)

Carbacephalosporin compounds of formula (I), STR1 salts thereof, processes for their synthesis and uses thereof, wherein: R1 is hydrogen, methoxy or formamido; R2 is an acyl group; CO2 R3 is a carboxy group or a carboxylate anion, or R3 is a carboxy protecting group or a pharmaceutically acceptable salt-forming group or in vivo hydrolysable ester group; R4, R5, R6 and R7 represent hydrogen or a substituent; R4 and R7 may be replaced by a chemical bond between the two carbon atoms shown; R5 and R6 may be linked together into a cyclic system. The compounds (I) have antibacterial properties.

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