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C23H33NO7 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1155868-37-3 Structure
  • Basic information

    1. Product Name: C23H33NO7
    2. Synonyms: C23H33NO7
    3. CAS NO:1155868-37-3
    4. Molecular Formula:
    5. Molecular Weight: 435.518
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1155868-37-3.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: C23H33NO7(CAS DataBase Reference)
    10. NIST Chemistry Reference: C23H33NO7(1155868-37-3)
    11. EPA Substance Registry System: C23H33NO7(1155868-37-3)
  • 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: 1155868-37-3(Hazardous Substances Data)

1155868-37-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1155868-37-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,5,8,6 and 8 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1155868-37:
(9*1)+(8*1)+(7*5)+(6*5)+(5*8)+(4*6)+(3*8)+(2*3)+(1*7)=183
183 % 10 = 3
So 1155868-37-3 is a valid CAS Registry Number.

1155868-37-3Downstream Products

1155868-37-3Relevant articles and documents

Synthesis of higher carbon sugars from dihydroxyacetone and d-arabinose: An organocatalytic approach

Cieplak, MacIej,Cmoch, Piotr,Jarosz, Slawomir,Ceborska, Magdalena

, p. 1213 - 1217,5 (2012/12/12)

The reaction of 2,3:4,5-diacetone-d-arabinose with protected dihydroxyacetone catalyzed by l-proline afforded two diastereoisomeric octoses in a 7:1 ratio in 75% yield. The anti (3S,4S) configuration at the newly created stereogenic centers was assigned to the main isomer on the basis of the X-ray analysis. The same reaction when catalyzed with unnatural d-proline provided the same products in a 1:20 ratio.

Organocatalytic syn-aldol reactions of dioxanones with (S)-isoserinal hydrate: Synthesis of L-deoxymannojirimycin and L-deoxyidonojirimycin

Palyam, Nagarjuna,Majewski, Marek

supporting information; experimental part, p. 4390 - 4392 (2009/09/06)

(Chemical Equation Presented) We report a new protocol for synthesis of L-1-deoxymannojirimycin, L-1-deoxyidonojirimycin, and the N-isopropyl derivative of the latter compound from the readily available precursors (S)-isoserinal hydrate and 2-tert-butyl-2

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