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208245-82-3

Carbamic acid, 1-pyrrolidinyl-, 1,1-dimethylethyl ester (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 208245-82-3 Structure

  • Basic information

    1. Product Name: Carbamic acid, 1-pyrrolidinyl-, 1,1-dimethylethyl ester (9CI)
    2. Synonyms: Carbamic acid, 1-pyrrolidinyl-, 1,1-dimethylethyl ester (9CI)
    3. CAS NO:208245-82-3
    4. Molecular Formula: C9H18N2O2
    5. Molecular Weight: 186.25142
    6. EINECS: N/A
    7. Product Categories: N-BOC
    8. Mol File: 208245-82-3.mol

  • Chemical Properties

    1. Melting Point: 110-114 °C
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.05±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 10.70±0.20(Predicted)
    10. CAS DataBase Reference: Carbamic acid, 1-pyrrolidinyl-, 1,1-dimethylethyl ester (9CI)(CAS DataBase Reference)
    11. NIST Chemistry Reference: Carbamic acid, 1-pyrrolidinyl-, 1,1-dimethylethyl ester (9CI)(208245-82-3)
    12. EPA Substance Registry System: Carbamic acid, 1-pyrrolidinyl-, 1,1-dimethylethyl ester (9CI)(208245-82-3)

  • 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: 208245-82-3(Hazardous Substances Data)

208245-82-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 208245-82-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,8,2,4 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 208245-82:
(8*2)+(7*0)+(6*8)+(5*2)+(4*4)+(3*5)+(2*8)+(1*2)=123
123 % 10 = 3
So 208245-82-3 is a valid CAS Registry Number.

208245-82-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Methyl-2-propanyl 1-pyrrolidinylcarbamate

1.2 Other means of identification

Product number -
Other names -

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:208245-82-3 SDS

208245-82-3Relevant articles and documents

N-Boc-O-tosyl hydroxylamine as a safe and efficient nitrogen source for the N-amination of aryl and alkyl amines: Electrophylic amination

Baburaj, Thankappan,Thambidurai, Sivalingam

, p. 1993 - 1996 (2011/10/08)

β-Boc-protected aryl and alkyl hydrazines, useful intermediates for azapeptides and N-substituted pyrazoles, were synthesized by electrophylic amination methodology, using less energetic N-Boc-O-tosyl hydroxylamine as an efficient nitrogen source. Also we have demonstrated a two-step, chromatography-free synthesis of N-Boc-O-tosyl hydroxylamine. Georg Thieme Verlag Stuttgart - New York.

The use of polyanions of hydrazines in the synthesis of heterocycles

Lebedev, Oleg,Bredihhin, Aleksei,T?upova, Svetlana,M?eorg, Uno

experimental part, p. 5438 - 5442 (2009/11/30)

A novel method for the synthesis of cyclic hydrazine derivatives is reported. The new method for the generation of nitrogen-containing heterocycles is based on a polyanion strategy. The described method provides a convenient access to cyclic hydrazine der

Use of polyanions for alkylation of hydrazine derivatives

Bredihhin, Aleksei,Maeeorg, Uno

, p. 4975 - 4977 (2008/03/28)

Alkylation of hydrazine and its derivatives still remains a quite complicated task. The novel method utilizing the polyanion strategy is reported. Formation and use of trianion for alkylation of hydrazine derivatives is first reported. Described method pr

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