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Aspartic acid, N,N-methylenebis(2-methyl-4,1-cyclohexanediyl)bis-, tetraethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • Aspartic acid,N,N'-[methylenebis(2-methyl-4,1-cyclohexanediyl)]bis-, 1,1',4,4'-tetraethylester

    Cas No: 136210-32-7

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  • 136210-32-7 Structure
  • Basic information

    1. Product Name: Aspartic acid, N,N-methylenebis(2-methyl-4,1-cyclohexanediyl)bis-, tetraethyl ester
    2. Synonyms: Aspartic acid, N,N-methylenebis(2-methyl-4,1-cyclohexanediyl)bis-, tetraethyl ester;Tetraethyl N,N'-[methylenebis(2-methyl-4,1-cyclohexane diyl)]bis(aspartate);bis(4-(1,2-bis(ethoxycarbonyl)ethylamino)-3-methylcyclohexyl)methane
    3. CAS NO:136210-32-7
    4. Molecular Formula: C31H54 N2 O8
    5. Molecular Weight: 582.77
    6. EINECS: 412-060-9
    7. Product Categories: N/A
    8. Mol File: 136210-32-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 634.6°Cat760mmHg
    3. Flash Point: 337.6°C
    4. Appearance: /
    5. Density: 1.1g/cm3
    6. Vapor Pressure: 5.2E-16mmHg at 25°C
    7. Refractive Index: 1.502
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 7.34±0.60(Predicted)
    11. Water Solubility: 5mg/L at 20℃
    12. CAS DataBase Reference: Aspartic acid, N,N-methylenebis(2-methyl-4,1-cyclohexanediyl)bis-, tetraethyl ester(CAS DataBase Reference)
    13. NIST Chemistry Reference: Aspartic acid, N,N-methylenebis(2-methyl-4,1-cyclohexanediyl)bis-, tetraethyl ester(136210-32-7)
    14. EPA Substance Registry System: Aspartic acid, N,N-methylenebis(2-methyl-4,1-cyclohexanediyl)bis-, tetraethyl ester(136210-32-7)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: 43-52/53
    3. Safety Statements: 36/37-61
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 136210-32-7(Hazardous Substances Data)

136210-32-7 Usage

Flammability and Explosibility

Nonflammable

Check Digit Verification of cas no

The CAS Registry Mumber 136210-32-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,2,1 and 0 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 136210-32:
(8*1)+(7*3)+(6*6)+(5*2)+(4*1)+(3*0)+(2*3)+(1*2)=87
87 % 10 = 7
So 136210-32-7 is a valid CAS Registry Number.
InChI:InChI=1/C31H54N2O8/c1-7-38-28(34)18-26(30(36)40-9-3)32-24-13-11-22(15-20(24)5)17-23-12-14-25(21(6)16-23)33-27(31(37)41-10-4)19-29(35)39-8-2/h20-27,32-33H,7-19H2,1-6H3

136210-32-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl 2-[[4-[[4-[(1,4-diethoxy-1,4-dioxobutan-2-yl)amino]-3-methylcyclohexyl]methyl]-2-methylcyclohexyl]amino]butanedioate

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:136210-32-7 SDS

136210-32-7Downstream Products

136210-32-7Relevant articles and documents

Method of preparing polyaspartic ester

-

Paragraph 0049-0058, (2020/04/29)

The invention discloses a method of preparing polyaspartic ester. The preparation method comprises the following steps: (1) organic primary amine and unsaturated dibasic acid ester are subjected to Michael addition reaction under the catalysis of a suppor

Method for preparing polyaspartic ester

-

Paragraph 0049; 0050; 0052-0058, (2019/10/01)

The invention discloses a method for preparing polyaspartic ester. According to the method, a supported zinc catalyst is used to catalyze a Michael addition reaction on organic primary amine and unsaturated binary acid ester. Reaction activity of primary

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