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CAS

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123802-17-5

4-benzyloxycarbonylamino-6-methylhept-1-en-3-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 123802-17-5 Structure

  • Basic information

    1. Product Name: 4-benzyloxycarbonylamino-6-methylhept-1-en-3-ol
    2. Synonyms: 4-benzyloxycarbonylamino-6-methylhept-1-en-3-ol
    3. CAS NO:123802-17-5
    4. Molecular Formula:
    5. Molecular Weight: 277.364
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 123802-17-5.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-benzyloxycarbonylamino-6-methylhept-1-en-3-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-benzyloxycarbonylamino-6-methylhept-1-en-3-ol(123802-17-5)
    11. EPA Substance Registry System: 4-benzyloxycarbonylamino-6-methylhept-1-en-3-ol(123802-17-5)

  • 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: 123802-17-5(Hazardous Substances Data)

123802-17-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 123802-17-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,8,0 and 2 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 123802-17:
(8*1)+(7*2)+(6*3)+(5*8)+(4*0)+(3*2)+(2*1)+(1*7)=95
95 % 10 = 5
So 123802-17-5 is a valid CAS Registry Number.

123802-17-5Relevant articles and documents

New Synthetic Methodology for the Synthesis of 7-Substituted Tetrahydroazepin-2-ones

Evans, P. Andrew,Holmes, Andrew B.,Russell, Keith

, p. 3397 - 3410 (2007/10/02)

The Claisen rearrangement of the vinyl substituted ketene aminals 2 (R = CH2CHMe2, CH2OSit-BuMe2) which were generated in situ by selenoxide elimination of the aminal precursors 3 in the presence of 1,8-diazabicycloundec-7-ene (DBU) furnished the enantiomerically pure 7-substituted tetrahydroazepin-2-ones 1.

N-ACYLAMINO ACID DERIVATIVES AND THEIR PHARMACEUTICAL COMPOSITIONS

-

, (2008/06/13)

An N-acylamino acid derivative of the formula: STR1 wherein the substituents are herein defined or a salt thereof, which is useful as hypotensive drugs.

Synthesis Of Homochiral Unsaturated Seven-Membered Lactams

Evans, P. Andrew,Holmes, Andrew B.,Russell, Keith

, p. 593 - 596 (2007/10/02)

The Claisen rearrangement of the vinyl substituted ketene aminals 6 which were generated in situ by selenoxide elimination of the aminal precursors 5 in the presence of 1,8-diazabicycloundec-7-ene (DBU) gave the homochiral unsaturated seven-membere

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