Welcome to LookChem.com Sign In|Join Free

CAS

  • or
methyl 4-(2-cyanopropan-2-yl)benzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

129488-73-9 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 129488-73-9 Structure
  • Basic information

    1. Product Name: methyl 4-(2-cyanopropan-2-yl)benzoate
    2. Synonyms: methyl 4-(2-cyanopropan-2-yl)benzoate;4-(Cyano-dimethyl-methyl)-benzoic acid methyl ester
    3. CAS NO:129488-73-9
    4. Molecular Formula: C12H13NO2
    5. Molecular Weight: 203.23712
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 129488-73-9.mol
  • Chemical Properties

    1. Melting Point: 45-50 °C
    2. Boiling Point: 323.0±25.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.084±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: Sealed in dry,Room Temperature
    8. Solubility: N/A
    9. CAS DataBase Reference: methyl 4-(2-cyanopropan-2-yl)benzoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl 4-(2-cyanopropan-2-yl)benzoate(129488-73-9)
    11. EPA Substance Registry System: methyl 4-(2-cyanopropan-2-yl)benzoate(129488-73-9)
  • 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: 129488-73-9(Hazardous Substances Data)

129488-73-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 129488-73-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,4,8 and 8 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 129488-73:
(8*1)+(7*2)+(6*9)+(5*4)+(4*8)+(3*8)+(2*7)+(1*3)=169
169 % 10 = 9
So 129488-73-9 is a valid CAS Registry Number.

129488-73-9Downstream Products

129488-73-9Relevant articles and documents

Synthesis of Tertiary Benzylic Nitriles via Nickel-Catalyzed Markovnikov Hydrocyanation of α-Substituted Styrenes

Xing, Yidan,Yu, Rongrong,Fang, Xianjie

, p. 1008 - 1012 (2020/02/04)

The Markovnikov hydrocyanation of α-substituted styrenes enables the synthesis of tertiary benzylic nitriles under nickel catalysis. The Lewis-acid-free transformation features an unprecedented functional groups tolerance, including the-OH and-NH2 groups. A broad range of tertiary benzylic nitriles were obtained in good to excellent yields. In addition, an asymmetric version of this reaction was preliminarily investigated.

Evaluation of thiazole containing biaryl analogs as diacylglycerol acyltransferase 1 (DGAT1) inhibitors

Kadam, Kishorkumar S.,Jadhav, Ravindra D.,Kandre, Shivaji,Guha, Tandra,Reddy, M. Mahesh Kumar,Brahma, Manoja K.,Deshmukh, Nitin J.,Dixit, Amol,Doshi, Lalit,Srinivasan, Shaila,Devle, Jayendra,Damre, Anagha,Nemmani, Kumar V. S.,Gupte, Amol,Sharma, Rajiv

, p. 337 - 347 (2013/10/01)

Biphenyl carboxylic acids, exemplified by compound 5, are known potent inhibitors of diacylglycerol acyltransferase, DGAT1, an enzyme involved in the final committed step of triglyceride biosynthesis. We have synthesized and evaluated 2-phenylthiazole, 4-

NOVEL SPIRO IMIDAZOLONES AS GLUCAGON RECEPTOR ANTAGONISTS, COMPOSITIONS, AND METHODS FOR THEIR USE

-

Page/Page column 167, (2011/10/13)

The present invention relates to compounds of the general formula: wherein ring A, ring B, R1, R3, Z, L1, and L2 are selected independently of each other and are as defined herein, to compositions comprising the compounds, and to methods of using the compounds as glucagon receptor antagonists and for the treatment or prevention of type 2 diabetes and conditions related thereto.

HETEROARYL COMPOUNDS AS DGAT-1 1NHIBITORS

-

Page/Page column 41, (2011/06/11)

The present invention relates to novel heteroaryl compounds, processes for their preparation, pharmaceutical compositions containing them and their use in the treatment of diseases or disorders mediated by Diacylglycerol acyltransferase (DGAT) enzyme, particularly DGAT- 1.

Synthesis of α-Aryl nitriles through palladium-catalyzed decarboxylative coupling of cyanoacetate salts with aryl halides and triflates

Shang, Rui,Ji, Dong-Sheng,Chu, Ling,Fu, Yao,Liu, Lei

supporting information; experimental part, p. 4470 - 4474 (2011/06/24)

Worth its salt: The palladium-catalyzed decarboxylative coupling of the cyanoacetate salt as well as its mono- and disubstituted derivatives with aryl chlorides, bromides, and triflates is described (see scheme). This reaction is potentially useful for the preparation of a diverse array of α-aryl nitriles and has good functional group tolerance. S-Phos=2-(2,6- dimethoxybiphenyl)dicyclohexylphosphine), Xant-Phos=4,5-bis(diphenylphosphino)- 9,9-dimethylxanthene. Copyright

CYCLYLAMINE DERIVATIVES AS CALCIUM CHANNEL BLOCKERS

-

Page/Page column 9, (2009/10/31)

Methods and compounds effective in ameliorating conditions characterized by unwanted calcium channel activity, particularly unwanted N-type and/or T-type calcium channel activity are disclosed. Specifically, a series of compounds of substituted or unsubstituted cyclylamine derivatives as shown in formulas (1).

ANTIVIRAL COMPOUNDS AND USE THEREOF

-

Page/Page column 31, (2009/12/02)

The invention relates to compounds, pharmaceutical compositions and methods useful for treating viral infection.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 129488-73-9