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  • 1078710-37-8 Structure
  • Basic information

    1. Product Name: C15H25N3O3
    2. Synonyms: C15H25N3O3
    3. CAS NO:1078710-37-8
    4. Molecular Formula:
    5. Molecular Weight: 295.382
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1078710-37-8.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: C15H25N3O3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C15H25N3O3(1078710-37-8)
    11. EPA Substance Registry System: C15H25N3O3(1078710-37-8)
  • 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: 1078710-37-8(Hazardous Substances Data)

1078710-37-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1078710-37-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,8,7,1 and 0 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1078710-37:
(9*1)+(8*0)+(7*7)+(6*8)+(5*7)+(4*1)+(3*0)+(2*3)+(1*7)=158
158 % 10 = 8
So 1078710-37-8 is a valid CAS Registry Number.

1078710-37-8Downstream Products

1078710-37-8Relevant articles and documents

Stereoselective alkylations of chiral nitro imine and nitro hydrazone dianions. Synthesis of enantiomerically enriched 3-substituted 1-nitrocyclohexenes

Denmark, Scott E.,Ares, Jeffrey J.

, p. 9647 - 9656 (2008)

(Chemical Equation Presented) Dianions of chiral nitro imines (generated by a combination of LDA and s-BuLi) underwent diastereoselective alkylation with methyl, butyl, isopropyl, allyl, and methallyl iodides. In contrast to the behavior of simple metalloenamines, the most selective auxiliary contained no coordinating groups but did possess a large steric difference between the two substituents. The yield and selectivity of the alkylations were improved by the addition of HMPA or DMPU. The use of (S)-1-naphthylethylamine as the auxiliary afforded the R absolute configuration of the alkylation products. This stereochemical outcome could be rationalized by simple steric approach controlled alkylation in a conformationally fixed, internally coordinated dianion. A SAMP nitro hydrazone gave poorer yields and selectivities.

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