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129840-78-4

3-Cyclohexene-1-carboxamide,5-hydroxy-N-methyl-,cis-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 129840-78-4 Structure

  • Basic information

    1. Product Name: 3-Cyclohexene-1-carboxamide,5-hydroxy-N-methyl-,cis-(9CI)
    2. Synonyms: 3-Cyclohexene-1-carboxamide,5-hydroxy-N-methyl-,cis-(9CI)
    3. CAS NO:129840-78-4
    4. Molecular Formula: C8H13NO2
    5. Molecular Weight: 155.19
    6. EINECS: N/A
    7. Product Categories: AMIDE
    8. Mol File: 129840-78-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 368.3±42.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.134±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 14.25±0.40(Predicted)
    10. CAS DataBase Reference: 3-Cyclohexene-1-carboxamide,5-hydroxy-N-methyl-,cis-(9CI)(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-Cyclohexene-1-carboxamide,5-hydroxy-N-methyl-,cis-(9CI)(129840-78-4)
    12. EPA Substance Registry System: 3-Cyclohexene-1-carboxamide,5-hydroxy-N-methyl-,cis-(9CI)(129840-78-4)

  • 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: 129840-78-4(Hazardous Substances Data)

129840-78-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 129840-78-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,8,4 and 0 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 129840-78:
(8*1)+(7*2)+(6*9)+(5*8)+(4*4)+(3*0)+(2*7)+(1*8)=154
154 % 10 = 4
So 129840-78-4 is a valid CAS Registry Number.

129840-78-4Downstream Products

129840-78-4Relevant articles and documents

Synthesis and Stereoselective Reduction of (+/-)-, (+)- and (-)-6-Substituted-6-azabicyclooctan-3-one

Pitner, J. Bruce,Abraham, Philip,Joo, Young J.,Triggle, David J.,Carroll, F. Ivy

, p. 1375 - 1381 (2007/10/02)

Starting with 6-oxabicyclooct-3-en-7-one 6, a three step, general synthetic route to both racemic and optically active 6-substituted 6-azabicyclooctan-3-ones has been developed.Opening of the lactone ring of 6 with amines gave amides which w

A concise synthesis of (±)-, (+)-, and (-)-6-methyl-6-azabicyclo[3. 2.1]octan-3α-ol

Philip, Abraham,Pitner, J. Bruce,Joo, Young J.,Triggle, David J.,Carroll, F. Ivy

, p. 984 - 985 (2007/10/02)

(±)-6-Methyl-6-azabicyclo[3.2.1]octan-3-one (1c) was prepared in three steps from 6-oxabicyclo[3.2.1]oct-3-en-7-one, and stereoselective reduction of (1c) provided (±)-6-methyl-6-azabicyclo[3.2.1]octan- 3α-ol (1a); adaptation of the sequence provided the

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