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1-<(S)-α-methylbenzylimino>-2,2-dimethylpropane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 33978-37-9 Structure
  • Basic information

    1. Product Name: 1-<(S)-α-methylbenzylimino>-2,2-dimethylpropane
    2. Synonyms: 1-<(S)-α-methylbenzylimino>-2,2-dimethylpropane
    3. CAS NO:33978-37-9
    4. Molecular Formula:
    5. Molecular Weight: 189.301
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 33978-37-9.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: 1-<(S)-α-methylbenzylimino>-2,2-dimethylpropane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-<(S)-α-methylbenzylimino>-2,2-dimethylpropane(33978-37-9)
    11. EPA Substance Registry System: 1-<(S)-α-methylbenzylimino>-2,2-dimethylpropane(33978-37-9)
  • 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: 33978-37-9(Hazardous Substances Data)

33978-37-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 33978-37-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,9,7 and 8 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 33978-37:
(7*3)+(6*3)+(5*9)+(4*7)+(3*8)+(2*3)+(1*7)=149
149 % 10 = 9
So 33978-37-9 is a valid CAS Registry Number.

33978-37-9Relevant articles and documents

One-pot solvent-free reductive amination with a solid ammonium carbamate salt from CO2 and amine

Kang, Philjun,Lee, Kyu Myung,Lee, Won Koo,Lee, Kyu Hyung,Lee, Byeongno,Cho, Jaeheung,Hur, Nam Hwi

, p. 46203 - 46207 (2015/02/19)

Many amines are liquid and their handling is inconvenient compared with the corresponding solids. We transformed a liquid (S)-(-)-1-phenylethylamine 1 to the corresponding neutral solid form 2 by reacting with carbon dioxide. We performed reductive aminat

Synthesis of chiral C2-symmetric 1,2-diamines by the addition of organolithium reagents to N,N'-bis[(S)-1-phenylethyl]ethanediimine

Martelli, Gianluca,Morri, Stefano,Savoia, Diego

, p. 8367 - 8374 (2007/10/03)

The additions of alkyl-, phenyl- and vinyllithium reagents to N,N'-bis[(S)-1-phenylethyl]ethanediimine in THF at -78°C and in DME at -60°C gave high yields of 1,2-diamines with low stereocontrol. Care was taken to quench the reaction mixtures with de-aera

Synthesis, enzymic degradation, lipophilic properties, and biological activity of [D-alanine2, t-butylglycine 5]enkephalin amide

Fauchere,Petermann

, p. 824 - 831 (2007/10/02)

L-C(a)-t-Butylglycine (Bug), its amide, methyl ester, and N(a)-t-butoxycarbonyl derivative were prepared by an asymmetric synthesis, and the Hansch side-chain hydrophobic (lipophilicity) parameter determined. A new enkephalin analogue, H . Tyr-D-Ala-Gly-Phe-Bug . HN2 was synthesized which is pharmacologically active in two in vitro assays and strongly resistant against a number of enzymes in vitro.

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