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4-Morpholinepropanoic acid, b-phenyl-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 127136-98-5 Structure
  • Basic information

    1. Product Name: 4-Morpholinepropanoic acid, b-phenyl-, ethyl ester
    2. Synonyms:
    3. CAS NO:127136-98-5
    4. Molecular Formula: C15H21NO3
    5. Molecular Weight: 263.337
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 127136-98-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-Morpholinepropanoic acid, b-phenyl-, ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-Morpholinepropanoic acid, b-phenyl-, ethyl ester(127136-98-5)
    11. EPA Substance Registry System: 4-Morpholinepropanoic acid, b-phenyl-, ethyl ester(127136-98-5)
  • 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: 127136-98-5(Hazardous Substances Data)

127136-98-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 127136-98-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,1,3 and 6 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 127136-98:
(8*1)+(7*2)+(6*7)+(5*1)+(4*3)+(3*6)+(2*9)+(1*8)=125
125 % 10 = 5
So 127136-98-5 is a valid CAS Registry Number.

127136-98-5Downstream Products

127136-98-5Relevant articles and documents

Guanidine-based task-specific ionic liquids as catalysts for aza-Michael addition under solvent-free conditions

Ying, Anguo,Zheng, Ming,Xu, Haidan,Qiu, Fangli,Ge, Changhua

experimental part, p. 883 - 890 (2012/04/17)

An efficient and facile protocol for aza-Michael addition of aliphatic and aromatic amines to electron-deficit alkenes using [TMG][Lac] as catalyst under solvent-free conditions was established.

Aza-Michael addition of aliphatic or aromatic amines to α,β-unsaturated compounds catalyzed by a DBU-derived ionic liquid under solvent-free conditions

Ying, An-Guo,Liu, Luo,Wu, Guo-Feng,Chen, Gang,Chen, Xin-Zhi,Ye, Wei-Dong

experimental part, p. 1653 - 1657 (2009/06/28)

A task-specific ionic liquid, 1,8-diazabicyclo[5.4.0]-undec-7-en-8-ium acetate has been successfully used as a catalyst for aza-conjugate addition of aliphatic or aromatic amines to various electron deficient alkenes under solvent-free conditions and at room temperature. The catalyst can be reused for six times without noticeable loss of activity.

ZrOCl2·8H2O on montmorillonite K10 accelerated conjugate addition of amines to α,β-unsaturated alkenes under solvent-free conditions

Hashemi, Mohammed M.,Eftekhari-Sis, Bagher,Abdollahifar, Amir,Khalili, Behzad

, p. 672 - 677 (2007/10/03)

At room temperature, ZrOCl2·8H2O on montmorillonite K10 efficiently catalyzes conjugate addition of amines to a variety of conjugated alkenes such as α,β-unsaturated carbonyl compounds, carboxylic esters, nitriles and amides under solvent-free conditions. The catalyst can be recycled for subsequent reactions without any appreciable loss of efficiency.

Water promoted Michael addition of secondary amines: To α,β- unsaturated carbonyl compounds under microwave irradiation

Matloubi Moghaddam, Firouz,Mohammadi, Mohsen,Hosseinnia, Azarmidocht

, p. 643 - 650 (2007/10/03)

A rapid Michael addition of secondary amines to α,β-unsaturated carbonyl compounds has been achieved in good to excellent yields in the presence of water under microwave irradiation. In the absence of water and under conventional method the reaction does not proceed or take place in very low yield after a long reaction time.

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