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2-Butyl-4-spirocyclopentane-2-imidazolin-5-one hydrochloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 151257-01-1 Structure
  • Basic information

    1. Product Name: 2-Butyl-4-spirocyclopentane-2-imidazolin-5-one hydrochloride
    2. Synonyms: [138402-05-8], C11H18N2O,194.14;1,3-Diazaspiro[4.4]non-1-en-4-one;2-butyl-, hydrochloride;2-n-Butyl-1;3-diaza-spiro[4;4]non-1-en-4-one HCl;F376 2-n-Butyl-1,3-diaza-spiro 4,4 non-1-en-4-one HCl;2-Butyl-4-spirocyclopentane-2-iMidazolin-5-one hyd
    3. CAS NO:151257-01-1
    4. Molecular Formula: C11H18N2O*ClH
    5. Molecular Weight: 230.73436
    6. EINECS: 424-560-4
    7. Product Categories: (intermediate of irbesartan);INTERMEDIATESOF;Irbesartan
    8. Mol File: 151257-01-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 328.6 °C at 760 mmHg
    3. Flash Point: 152.6 °C
    4. Appearance: white or pale white crystal powder
    5. Density: N/A
    6. Vapor Pressure: 0.000135mmHg at 25°C
    7. Refractive Index: N/A
    8. Storage Temp.: Inert atmosphere,Room Temperature
    9. Solubility: N/A
    10. Water Solubility: Soluble in water
    11. CAS DataBase Reference: 2-Butyl-4-spirocyclopentane-2-imidazolin-5-one hydrochloride(CAS DataBase Reference)
    12. NIST Chemistry Reference: 2-Butyl-4-spirocyclopentane-2-imidazolin-5-one hydrochloride(151257-01-1)
    13. EPA Substance Registry System: 2-Butyl-4-spirocyclopentane-2-imidazolin-5-one hydrochloride(151257-01-1)
  • 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: 151257-01-1(Hazardous Substances Data)

151257-01-1 Usage

Chemical Properties

Oil

Check Digit Verification of cas no

The CAS Registry Mumber 151257-01-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,2,5 and 7 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 151257-01:
(8*1)+(7*5)+(6*1)+(5*2)+(4*5)+(3*7)+(2*0)+(1*1)=101
101 % 10 = 1
So 151257-01-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H18N2O.ClH/c1-2-3-6-9-12-10(14)11(13-9)7-4-5-8-11;/h2-8H2,1H3,(H,12,13,14);1H

151257-01-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Butyl-1,3-diazaspiro[4.4]non-1-en-4-one Hydrochloride

1.2 Other means of identification

Product number -
Other names 2-BUTYL-1,3-DIAZASPIRO(4.4)NON-1-EN-4-ONE HYDROCHLORIDE

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:151257-01-1 SDS

151257-01-1Downstream Products

151257-01-1Relevant articles and documents

Process for the preparation of 4-oxoimidazolinium salts

-

, (2008/06/13)

4-Oxoimidazolinium salts of the general formula: STR1 wherein R1 and R2 independently of one another are C1-10 -alkyl, C2-10 -alkenyl, C3-7 -cycloalkyl or optionally substituted aryl, arylalkyl, heteroaryl or heteroarylalkyl, or R1 and R2, together with the carbon atom to which they are bonded, form a three-membered to seven-membered saturated or unsaturated carbocyclic or heterocyclic ring, R3 is a C1-10 -alkyl group, C1-10 -alkenyl group, C3-7 -cycloalkyl group, aryl group, arylalkyl group or heteroaryl group, and A-- is an anion of a strong acid, are prepared by the cyclization of an α-acylaminonitrile in a nonaqueous solvent, in the presence of a lower alcohol and a strong acid. The compounds are intermediates for pharmaceutical active substances, for example, angiotensin II antagonists.

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