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dimethyl 4-cyano-4-(3,4-dimethoxyphenyl)heptanedioate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 61330-09-4 Structure
  • Basic information

    1. Product Name: dimethyl 4-cyano-4-(3,4-dimethoxyphenyl)heptanedioate
    2. Synonyms: dimethyl 4-cyano-4-(3,4-dimethoxyphenyl)heptanedioate
    3. CAS NO:61330-09-4
    4. Molecular Formula: C18H23NO6
    5. Molecular Weight: 349.37832
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 61330-09-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: dimethyl 4-cyano-4-(3,4-dimethoxyphenyl)heptanedioate(CAS DataBase Reference)
    10. NIST Chemistry Reference: dimethyl 4-cyano-4-(3,4-dimethoxyphenyl)heptanedioate(61330-09-4)
    11. EPA Substance Registry System: dimethyl 4-cyano-4-(3,4-dimethoxyphenyl)heptanedioate(61330-09-4)
  • 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: 61330-09-4(Hazardous Substances Data)

61330-09-4 Usage

Preparation

Dimethyl 4-cyano-4-(3,4-dimethoxyphenyl)heptanedioate can be prepared by the following steps:A mixture of finely powdered 3,4- dimethoxyphenylacetonitrile 45 (5 g, 28.25 mmol) and ?TBAHSO4 (0.096 g, 0.28 mmol) in 10% aq. NaOH ?solution (20 ml) was stirred for 30 minutes at room ?temperature. A dark red colour appeared. The mixture was ?then cooled in an ice-bath. Methyl acrylate 239 was slowly ?added dropwise at 0 o C, (12.65 ml, 138.95 mmol). After 1 hour a colourless solid was ?formed, which was filtered and crystallized from EtOAc (7.49 g, 76% yield). ? Alternatively, dimethyl 4-cyano-4-(3,4-dimethoxyphenyl)heptanedioate was prepared by refluxing a mixture of 3,4- dimethoxyphenylacetonitrile (100 g, 0.564 mol) and methyl acrylate (253 ml, 2.82 mol) in ?the presence of Triton-B (2.35 ml, 0.006 mol, 40% solution in MeOH) in CH3CN for ?overnight in almost quantitative yields (197 g).

Check Digit Verification of cas no

The CAS Registry Mumber 61330-09-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,3,3 and 0 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 61330-09:
(7*6)+(6*1)+(5*3)+(4*3)+(3*0)+(2*0)+(1*9)=84
84 % 10 = 4
So 61330-09-4 is a valid CAS Registry Number.

61330-09-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl 4-cyano-4-(3,4-dimethoxyphenyl)heptanedioate

1.2 Other means of identification

Product number -
Other names -

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:61330-09-4 SDS

61330-09-4Relevant articles and documents

A simple and efficient synthesis of (±)-mesembrine

Chavan, Subhash P.,Khobragade, Dushant A.,Pathak, Ashok B.,Kalkote

, p. 5263 - 5265 (2007/10/03)

A simple and efficient synthesis of (±)-mesembrine 1 is described employing double Michael addition and as the key step in 18% overall yield.

Verapamil analogues with restricted molecular flexibility

Dei,Romanelli,Scapecchi,Teodori,Chiarini,Gualtieri

, p. 2219 - 2225 (2007/10/02)

Three analogues with restricted flexibility were designed to study the active conformation of verapamil during interaction with the slow calcium channel. Thus cis- and trans-1-(3,4-dimethoxyphenyl)-4-[N-[2-(3,4-dimethoxyphenyl)ethyl]-N-me thylamino]-r-1-c

Bisarylamines

-

, (2008/06/13)

Compounds of the formula: STR1 and pharmaceutically acceptable salts thereof, wherein: Ar is phenyl, naphthyl, heteroaryl, indole, or fused arylcycloalkyl optionally substituted with hydroxy, halo, CF 3, NO 2, C 1-6 alkyl, C 1-6 alkoxy or aryloxy;A and A'

SYNTHESIS OF ALKALOIDS, TORTUOSAMINE, N-FORMYLTORTUOSAMINE, AND RELATED COMPOUND

Koyama, Junko,Sugita, Teruyo,Suzuta, Yukio,Irie, Hiroshi

, p. 969 - 972 (2007/10/02)

Synthesis of alkaloids, tortuosamine, N-formyltortuosamine, and related compound, was accomplished by application of a new method constructing cycloalkenopyridines by thermal rearrangement of oxime O-allyl ethers as a key step

4-Arylcyclohexylamines

-

, (2008/06/13)

The invention relates to novel 4-hydroxymethyl(acyloxymethyl and methyl)-4-arylcyclohexylamines embraced by the formula SPC1 Wherein Ar is an aromatic ring selected from the group consisting of phenyl and naphthyl, each of which has from zero through three substituents independently selected from the group consisting of fluorine, chlorine, bromine, lower alkyl of one through three carbon atoms, lower alkoxy of one through three carbon atoms, and lower alkylthio of one through three carbon atoms; Z is selected from the group consisting of hydrogen, hydroxy and lower acyloxy of one through four carbon atoms; ? is a generic expression denoting cis and trans stereoconfiguration and mixtures thereof, with the proviso that when the stereoconfiguration of the linkage connecting the cyclohexane ring and CH2 Z is cis to the amino group, the linkage connecting the cyclohexane and Ar rings is trans, and vice versa; R1 is selected from the group consisting of hydrogen and lower alkyl of one through three carbon atoms; R2 is selected from the group consisting of hydrogen, lower alkyl of one through three carbon atoms, EQU1 WHEREIN N IS 2 THROUGH 5 AND Ar has the same meaning as above; R1 and R2 taken together with --N is a saturated heterocyclic amino radical selected from the group consisting of unsubstituted and substituted pyrrolidino, piperidino, hexamethylenimino, morpholino and piperazino; and pharmacologically acceptable acid addition salts thereof. It also relates to intermediates and processes for the preparation of the aforesaid novel compounds (I) and novel derivatives thereof. The administration to humans and animals of the novel compounds (I) depresses their central nervous systems and lowers their blood pressures.

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