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3-Pyridinecarbonyl chloride, 1,6-dihydro-1-methyl-6-oxo- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 162330-16-7 Structure
  • Basic information

    1. Product Name: 3-Pyridinecarbonyl chloride, 1,6-dihydro-1-methyl-6-oxo- (9CI)
    2. Synonyms: 3-Pyridinecarbonyl chloride, 1,6-dihydro-1-methyl-6-oxo- (9CI);1-Methyl-6-oxo-1,6-dihydropyridine-3-carbonyl chloride;1,6-DIHYDRO-1-METHYL-6-OXO-3-PYRIDINECARBONYL CHLORIDE
    3. CAS NO:162330-16-7
    4. Molecular Formula: C7H6ClNO2
    5. Molecular Weight: 171.58104
    6. EINECS: N/A
    7. Product Categories: ACIDHALIDE
    8. Mol File: 162330-16-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 294.4±29.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.375±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: -1.98±0.62(Predicted)
    10. CAS DataBase Reference: 3-Pyridinecarbonyl chloride, 1,6-dihydro-1-methyl-6-oxo- (9CI)(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-Pyridinecarbonyl chloride, 1,6-dihydro-1-methyl-6-oxo- (9CI)(162330-16-7)
    12. EPA Substance Registry System: 3-Pyridinecarbonyl chloride, 1,6-dihydro-1-methyl-6-oxo- (9CI)(162330-16-7)
  • 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: 162330-16-7(Hazardous Substances Data)

162330-16-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 162330-16-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,2,3,3 and 0 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 162330-16:
(8*1)+(7*6)+(6*2)+(5*3)+(4*3)+(3*0)+(2*1)+(1*6)=97
97 % 10 = 7
So 162330-16-7 is a valid CAS Registry Number.

162330-16-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methyl-6-oxopyridine-3-carbonyl chloride

1.2 Other means of identification

Product number -
Other names 1-methyl-6-oxo-1,6-dihydropyridine-3-carbonyl chloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:162330-16-7 SDS

162330-16-7Downstream Products

162330-16-7Relevant articles and documents

COMPOUNDS AND USES THEREOF

-

, (2020/10/20)

The present invention features compounds useful in the treatment of neurological disorders and primary brain cancer. The compounds of the invention, alone or in combination with other pharmaceutically active agents, can be used for treating or preventing neurological disorders and primary brain cancer.

COMPOUNDS AND USES THEREOF

-

, (2019/10/15)

The present invention features compounds useful in the treatment of neurological disorders. The compounds of the invention, alone or in combination with other pharmaceutically active agents, can be used for treating or preventing neurological disorders.

Novel 5α-reductase inhibitors. Synthesis and structure-activity studies of 5-substituted 1-methyl-2-pyridones and 1-methyl-2-piperidones

Hartmann, R. W.,Reichert, M.,Goehring, S.

, p. 807 - 818 (2007/10/02)

In search for nonsteroidal inhibitors of 5α-reductase for the treatment of benign prostatic hyperplasia (BPH) and possibly prostate cancer, substrate mimicks were synthesized comprising of a 1-methyl-2-pyridone (2, 4-16) or 1-methyl-2-piperidone (1, 3, 17

Substituent Effects in Non-Aromatic Nitrogen Heterocycles: Alkaline Hydrolysis of Methyl N-Methyl(oxo)dihydropyridinecarboxylates and Diaza Analogues

Deady, Leslie W.

, p. 637 - 641 (2007/10/02)

Ester hydrolysis studies on some isomeric methoxycarbonyl derivatives of N-methylpyridin-2- and 4-ones show that reaction rates are affected by the relative positions of CO2Me, =O and NMe functions in ways which could not be predicted.However, from limited results for analogous pyrimidine derivatives, it seems that reactivity in these polyfunctional compounds can be predicted from the pyridine data by assuming additivity of effects.

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