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CAS

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206348-65-4

Carbamic acid, (tetrahydro-5-oxo-3-furanyl)-, 1,1-dimethylethyl ester (9CI), also known as Carbetamide, is a chemical compound with the molecular formula C11H17NO3. It is a widely used herbicide in agricultural settings for controlling grasses and weeds.
Used in Agricultural Industry:
Carbamic acid, (tetrahydro-5-oxo-3-furanyl)-, 1,1-dimethylethyl ester (9CI) is used as a pre-emergent herbicide for controlling grasses and weeds in various agricultural settings. It works by inhibiting the growth of young seedling grasses and has a selective effect on certain types of plants, making it a valuable tool for crop protection.
Used in Crop Protection:
Carbamic acid, (tetrahydro-5-oxo-3-furanyl)-, 1,1-dimethylethyl ester (9CI) is used as a herbicide for crop protection. Its selective effect on certain types of plants allows for effective control of unwanted grasses and weeds without harming the desired crops. This selective action makes it a useful tool in maintaining healthy and productive agricultural fields.

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  • Carbamic acid, (tetrahydro-5-oxo-3-furanyl)-, 1,1-dimethylethyl ester (9CI)

    Cas No: 206348-65-4

  • USD $ 1.9-2.9 / Gram

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  • 206348-65-4 Structure

  • Basic information

    1. Product Name: Carbamic acid, (tetrahydro-5-oxo-3-furanyl)-, 1,1-dimethylethyl ester (9CI)
    2. Synonyms: Carbamic acid, (tetrahydro-5-oxo-3-furanyl)-, 1,1-dimethylethyl ester (9CI);tert-Butyl (5-oxotetrahydrofuran-3-yl)carbaMate;Tert-Butyl (5-Oxotetrahydrofuran-3-Yl)Carbamate(WXC01708)
    3. CAS NO:206348-65-4
    4. Molecular Formula: C9H15NO4
    5. Molecular Weight: 201.2197
    6. EINECS: N/A
    7. Product Categories: N-BOC
    8. Mol File: 206348-65-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 363.7±31.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.15±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. PKA: 11.08±0.20(Predicted)
    10. CAS DataBase Reference: Carbamic acid, (tetrahydro-5-oxo-3-furanyl)-, 1,1-dimethylethyl ester (9CI)(CAS DataBase Reference)
    11. NIST Chemistry Reference: Carbamic acid, (tetrahydro-5-oxo-3-furanyl)-, 1,1-dimethylethyl ester (9CI)(206348-65-4)
    12. EPA Substance Registry System: Carbamic acid, (tetrahydro-5-oxo-3-furanyl)-, 1,1-dimethylethyl ester (9CI)(206348-65-4)

  • 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: 206348-65-4(Hazardous Substances Data)

206348-65-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 206348-65-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,6,3,4 and 8 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 206348-65:
(8*2)+(7*0)+(6*6)+(5*3)+(4*4)+(3*8)+(2*6)+(1*5)=124
124 % 10 = 4
So 206348-65-4 is a valid CAS Registry Number.

206348-65-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3(R)-[(t-butoxycarbonyl) - amino]-γ-butyrolactone

1.2 Other means of identification

Product number -
Other names 3(S)-[(t-butoxycarbonyl)amino]-γ-butyrolactone

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:206348-65-4 SDS

206348-65-4Downstream Products

206348-65-4Relevant articles and documents

A new approach to the synthesis of functionalized pyrido[2,3-b]indoles by way of a palladium-catalyzed ring closing reaction between the N-1 and C- 9a positions

Abouabdellah, Ahmed,Dodd, Robert H.

, p. 2119 - 2122 (2007/10/03)

The enolate of 4-N-(tert-butyloxycarbonyl)aminobutyro-γ-lactone 9 reacted with 2-bromo-1methylindole-3-carboxaldehyde in the presence of stannic chloride to give the product of aldol condensation 16. Deprotection and dehydration of the latter with trifluo

Isoindoline derivatives

-

, (2008/06/13)

Optically active 8-methoxyquinolonecarboxylic acids represented by the formula (I) wherein R1 is lower alkyl have been found to possess potent antibacterial activity against both Gram-negative and Gram-positive bacteria. The compounds may be synthesized from novel optically active intermediates.

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