Welcome to LookChem.com Sign In|Join Free

CAS

  • or
DIMETHYL 3-METHYLGLUTACONATE is an organic compound that has been demonstrated to induce oxidative damage in specific tissues, such as the striatum and liver in rats. It is also utilized in the synthesis of insect growth regulators that exhibit juvenile hormone activity, making it a versatile compound with applications in both biological research and pest control.

52313-87-8 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 52313-87-8 Structure
  • Basic information

    1. Product Name: DIMETHYL 3-METHYLGLUTACONATE
    2. Synonyms: DIMETHYL 3-METHYLGLUTACONATE;2-Pentenedioic acid, 3-methyl-, dimethyl ester;Dimethyl (2E)-2-methyl-2-pentenedioate;dimethyl 3-methylglutaconate, mixture of ci;Dimethyl 3-methylglutaconate,mixture of cis and trans;dimethyl 3-methylpent-2-enedioate;DIMETHYL 3-METHYLGLUTACONATE, 95%, MIXTU RE OF CIS AND TRANS;3-Methyl-2-pentenedioic acid dimethyl ester
    3. CAS NO:52313-87-8
    4. Molecular Formula: C8H12O4
    5. Molecular Weight: 172.18
    6. EINECS: 257-839-2
    7. Product Categories: C8 to C9;Carbonyl Compounds;Esters
    8. Mol File: 52313-87-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 109-110 °C12 mm Hg(lit.)
    3. Flash Point: 208 °F
    4. Appearance: /
    5. Density: 1.095 g/mL at 25 °C(lit.)
    6. Vapor Pressure: 0.0579mmHg at 25°C
    7. Refractive Index: n20/D 1.456(lit.)
    8. Storage Temp.: 2-8°C
    9. Solubility: Chloroform, Methanol
    10. CAS DataBase Reference: DIMETHYL 3-METHYLGLUTACONATE(CAS DataBase Reference)
    11. NIST Chemistry Reference: DIMETHYL 3-METHYLGLUTACONATE(52313-87-8)
    12. EPA Substance Registry System: DIMETHYL 3-METHYLGLUTACONATE(52313-87-8)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 52313-87-8(Hazardous Substances Data)

52313-87-8 Usage

Uses

Used in Biological Research:
DIMETHYL 3-METHYLGLUTACONATE is used as an inducer of oxidative damage for [application reason] studying the effects of oxidative stress on tissues like the striatum and liver in rats. This application helps researchers understand the mechanisms behind oxidative damage and develop potential treatments or preventive measures.
Used in Pest Control Industry:
DIMETHYL 3-METHYLGLUTACONATE is used as a precursor in the preparation of insect growth regulators for [application reason] controlling insect populations by disrupting their growth and development. The juvenile hormone activity of the resulting compounds makes them effective in managing pests, reducing the need for chemical pesticides and promoting more sustainable agricultural practices.

Check Digit Verification of cas no

The CAS Registry Mumber 52313-87-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,3,1 and 3 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 52313-87:
(7*5)+(6*2)+(5*3)+(4*1)+(3*3)+(2*8)+(1*7)=98
98 % 10 = 8
So 52313-87-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H12O4/c1-6(4-7(9)11-2)5-8(10)12-3/h4H,5H2,1-3H3/b6-4-

52313-87-8SDS

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 Dimethyl 3-methylpent-2-enedioate

1.2 Other means of identification

Product number -
Other names 2-Pentenedioic acid, 3-methyl-, dimethyl ester

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:52313-87-8 SDS

52313-87-8Synthetic route

methyl 4,6-dimethyl-2-oxo-2H-pyran-5-carboxylate
41264-06-6

methyl 4,6-dimethyl-2-oxo-2H-pyran-5-carboxylate

sodium methylate
124-41-4

sodium methylate

3-methyl-2-pentene-1,5-diacid dimethyl
52313-87-8

3-methyl-2-pentene-1,5-diacid dimethyl

Conditions
ConditionsYield
In methanol
3-Hydroxy-3-methyl-5,5-bis-methylsulfanyl-pent-4-enoic acid ethyl ester

3-Hydroxy-3-methyl-5,5-bis-methylsulfanyl-pent-4-enoic acid ethyl ester

3-methyl-2-pentene-1,5-diacid dimethyl
52313-87-8

3-methyl-2-pentene-1,5-diacid dimethyl

Conditions
ConditionsYield
With boron trifluoride diethyl etherate In methanol for 20h; Heating; Yield given;
methanol
67-56-1

methanol

3-methylpent-2-enedioic acid
372-42-9, 15649-56-6, 5746-90-7

3-methylpent-2-enedioic acid

3-methyl-2-pentene-1,5-diacid dimethyl
52313-87-8

3-methyl-2-pentene-1,5-diacid dimethyl

Conditions
ConditionsYield
With sulfuric acid
Stage #1: 3-methylpent-2-enedioic acid at 72℃; for 8h;
Stage #2: methanol at 90 - 120℃; for 0.5h;
485 g
3-methyl-2-pentene-1,5-diacid dimethyl
52313-87-8

3-methyl-2-pentene-1,5-diacid dimethyl

dimethyl 3-methylglutarate
19013-37-7

dimethyl 3-methylglutarate

Conditions
ConditionsYield
With hydrogen; palladium on activated charcoal at 65℃; under 3040 Torr;91%
3-methyl-2-pentene-1,5-diacid dimethyl
52313-87-8

3-methyl-2-pentene-1,5-diacid dimethyl

pivalaldehyde
630-19-3

pivalaldehyde

anti-6-tert-butyl-5-methoxycarbonyl-4-methyl-5,6-dihydro-2H-pyran-2-one

anti-6-tert-butyl-5-methoxycarbonyl-4-methyl-5,6-dihydro-2H-pyran-2-one

Conditions
ConditionsYield
With zinc(II) chloride; lithium hexamethyldisilazane In tetrahydrofuran 1.) -35 deg C, 0.5 h, 2.) -65 deg C, 15 min, 3.) -30 deg C to -10 deg C, 7 h;90%
3-methyl-2-pentene-1,5-diacid dimethyl
52313-87-8

3-methyl-2-pentene-1,5-diacid dimethyl

phenylacetaldehyde
122-78-1

phenylacetaldehyde

(Z)-3-Methyl-2-((E)-styryl)-pent-2-enedioic acid 1-methyl ester
135628-90-9

(Z)-3-Methyl-2-((E)-styryl)-pent-2-enedioic acid 1-methyl ester

Conditions
ConditionsYield
With sodium methylate In diethyl ether at 20℃; for 2h;85%
Diphenylacetaldehyde
947-91-1

Diphenylacetaldehyde

3-methyl-2-pentene-1,5-diacid dimethyl
52313-87-8

3-methyl-2-pentene-1,5-diacid dimethyl

(Z)-2-(2,2-Diphenyl-vinyl)-3-methyl-pent-2-enedioic acid 1-methyl ester
135628-95-4

(Z)-2-(2,2-Diphenyl-vinyl)-3-methyl-pent-2-enedioic acid 1-methyl ester

Conditions
ConditionsYield
With sodium methylate In diethyl ether at 20℃; for 2h;65%
4-Methoxyphenylacetaldehyde
5703-26-4

4-Methoxyphenylacetaldehyde

3-methyl-2-pentene-1,5-diacid dimethyl
52313-87-8

3-methyl-2-pentene-1,5-diacid dimethyl

(Z)-2-[(E)-2-(4-Methoxy-phenyl)-vinyl]-3-methyl-pent-2-enedioic acid 1-methyl ester
135628-92-1

(Z)-2-[(E)-2-(4-Methoxy-phenyl)-vinyl]-3-methyl-pent-2-enedioic acid 1-methyl ester

Conditions
ConditionsYield
With sodium methylate In diethyl ether at 20℃; for 2h;65%
3-methyl-2-pentene-1,5-diacid dimethyl
52313-87-8

3-methyl-2-pentene-1,5-diacid dimethyl

2-Phenylpropanal
34713-70-7

2-Phenylpropanal

(Z)-3-Methyl-2-((E)-2-phenyl-propenyl)-pent-2-enedioic acid 1-methyl ester
135628-94-3

(Z)-3-Methyl-2-((E)-2-phenyl-propenyl)-pent-2-enedioic acid 1-methyl ester

Conditions
ConditionsYield
With sodium methylate In diethyl ether at 20℃; for 2h;65%
3-methyl-2-pentene-1,5-diacid dimethyl
52313-87-8

3-methyl-2-pentene-1,5-diacid dimethyl

phenylacetaldehyde
122-78-1

phenylacetaldehyde

syn-6-benzyl-5-methoxycarbonyl-4-methyl-5,6-dihydro-2H-pyran-2-one

syn-6-benzyl-5-methoxycarbonyl-4-methyl-5,6-dihydro-2H-pyran-2-one

Conditions
ConditionsYield
With zinc(II) chloride; lithium hexamethyldisilazane In tetrahydrofuran 1.) -35 deg C, 0.5 h, 2.) -65 deg C, 15 min, 3.) -30 deg C to -10 deg C, 7 h;65%
3-methyl-2-pentene-1,5-diacid dimethyl
52313-87-8

3-methyl-2-pentene-1,5-diacid dimethyl

4-methylphenylacetaldehyde
104-09-6

4-methylphenylacetaldehyde

(Z)-3-Methyl-2-((E)-2-p-tolyl-vinyl)-pent-2-enedioic acid 1-methyl ester
135628-91-0

(Z)-3-Methyl-2-((E)-2-p-tolyl-vinyl)-pent-2-enedioic acid 1-methyl ester

Conditions
ConditionsYield
With sodium methylate In diethyl ether at 20℃; for 2h;60%
3-methyl-2-pentene-1,5-diacid dimethyl
52313-87-8

3-methyl-2-pentene-1,5-diacid dimethyl

4-fluorophenylacetaldehyde
1736-67-0

4-fluorophenylacetaldehyde

(Z)-2-[(E)-2-(4-Fluoro-phenyl)-vinyl]-3-methyl-pent-2-enedioic acid 1-methyl ester
135628-93-2

(Z)-2-[(E)-2-(4-Fluoro-phenyl)-vinyl]-3-methyl-pent-2-enedioic acid 1-methyl ester

Conditions
ConditionsYield
With sodium methylate In diethyl ether at 20℃; for 2h;60%
3-methyl-2-pentene-1,5-diacid dimethyl
52313-87-8

3-methyl-2-pentene-1,5-diacid dimethyl

salicylaldehyde
90-02-8

salicylaldehyde

methyl (E)-3-(2-oxo-2H-1-benzopyran-3-yl)-2-butenoate

methyl (E)-3-(2-oxo-2H-1-benzopyran-3-yl)-2-butenoate

Conditions
ConditionsYield
With piperidine In benzene at 80℃; for 45h;55%
3-methyl-2-pentene-1,5-diacid dimethyl
52313-87-8

3-methyl-2-pentene-1,5-diacid dimethyl

3,4-Dimethyl-5-(2-nitroethyl)-pyrrol-2-carbonsaeure-tert-butylester
80053-00-5

3,4-Dimethyl-5-(2-nitroethyl)-pyrrol-2-carbonsaeure-tert-butylester

3,4-Dimethyl-5-(3,3-bis-methoxycarbonylmethyl-2-nitrobutyl)-pyrrol-2-carbonsaeure-tert-butylester
90702-48-0

3,4-Dimethyl-5-(3,3-bis-methoxycarbonylmethyl-2-nitrobutyl)-pyrrol-2-carbonsaeure-tert-butylester

Conditions
ConditionsYield
46%
3-methyl-2-pentene-1,5-diacid dimethyl
52313-87-8

3-methyl-2-pentene-1,5-diacid dimethyl

benzaldehyde
100-52-7

benzaldehyde

5-methoxycarbonyl-4-methyl-6-phenyl-5,6-dihydro-2H-pyran-2-one

5-methoxycarbonyl-4-methyl-6-phenyl-5,6-dihydro-2H-pyran-2-one

Conditions
ConditionsYield
With zinc(II) chloride; lithium hexamethyldisilazane In tetrahydrofuran 1.) -35 deg C, 0.5 h, 2.) -65 deg C, 15 min, 3.) -30 deg C to -10 deg C, 7 h;31%
methanol
67-56-1

methanol

3-methyl-2-pentene-1,5-diacid dimethyl
52313-87-8

3-methyl-2-pentene-1,5-diacid dimethyl

4-chlorophenyldiazonium salt
17333-85-6

4-chlorophenyldiazonium salt

1-(4-chloro-phenyl)-4-methyl-6-oxo-1,6-dihydro-pyridazine-3-carboxylic acid methyl ester
100375-28-8

1-(4-chloro-phenyl)-4-methyl-6-oxo-1,6-dihydro-pyridazine-3-carboxylic acid methyl ester

Conditions
ConditionsYield
With sodium methylate; sodium acetate
nonan-1-al
124-19-6

nonan-1-al

3-methyl-2-pentene-1,5-diacid dimethyl
52313-87-8

3-methyl-2-pentene-1,5-diacid dimethyl

4-methyl-2-octyl-6-oxo-3,6-dihydro-2H-pyran-3-carboxylic acid
131591-88-3

4-methyl-2-octyl-6-oxo-3,6-dihydro-2H-pyran-3-carboxylic acid

Conditions
ConditionsYield
With potassium hydroxide
benzenediazonium
2684-02-8

benzenediazonium

3-methyl-2-pentene-1,5-diacid dimethyl
52313-87-8

3-methyl-2-pentene-1,5-diacid dimethyl

4-methyl-6-oxo-1-phenyl-1,6-dihydro-pyridazine-3-carboxylic acid methyl ester
107516-97-2

4-methyl-6-oxo-1-phenyl-1,6-dihydro-pyridazine-3-carboxylic acid methyl ester

Conditions
ConditionsYield
With sodium methylate; sodium acetate
heptanal
111-71-7

heptanal

3-methyl-2-pentene-1,5-diacid dimethyl
52313-87-8

3-methyl-2-pentene-1,5-diacid dimethyl

4-heptylidene-3-methyl-pentenedioic acid

4-heptylidene-3-methyl-pentenedioic acid

Conditions
ConditionsYield
With potassium hydroxide beim Behandeln des danach isolierten Salzes in wss. Loesung mit konz. wss. Salzsaeure;
heptanal
111-71-7

heptanal

3-methyl-2-pentene-1,5-diacid dimethyl
52313-87-8

3-methyl-2-pentene-1,5-diacid dimethyl

2-hexyl-4-methyl-6-oxo-3,6-dihydro-2H-pyran-3-carboxylic acid
108996-63-0

2-hexyl-4-methyl-6-oxo-3,6-dihydro-2H-pyran-3-carboxylic acid

Conditions
ConditionsYield
With potassium hydroxide
p-methoxybenzenediazonium
17333-79-8

p-methoxybenzenediazonium

3-methyl-2-pentene-1,5-diacid dimethyl
52313-87-8

3-methyl-2-pentene-1,5-diacid dimethyl

1-(4-methoxy-phenyl)-4-methyl-6-oxo-1,6-dihydro-pyridazine-3-carboxylic acid methyl ester
100870-84-6

1-(4-methoxy-phenyl)-4-methyl-6-oxo-1,6-dihydro-pyridazine-3-carboxylic acid methyl ester

Conditions
ConditionsYield
With sodium methylate; sodium acetate
4-methylbenzene diazonium
57573-52-1

4-methylbenzene diazonium

3-methyl-2-pentene-1,5-diacid dimethyl
52313-87-8

3-methyl-2-pentene-1,5-diacid dimethyl

A

4-methyl-6-oxo-1-p-tolyl-1,6-dihydro-pyridazine-3-carboxylic acid methyl ester
106378-47-6

4-methyl-6-oxo-1-p-tolyl-1,6-dihydro-pyridazine-3-carboxylic acid methyl ester

B

3-methyl-4-p-tolylhydrazono-pentenedioic acid dimethyl ester
109506-29-8

3-methyl-4-p-tolylhydrazono-pentenedioic acid dimethyl ester

Conditions
ConditionsYield
With sodium methylate; sodium acetate
4-methylbenzene diazonium
57573-52-1

4-methylbenzene diazonium

3-methyl-2-pentene-1,5-diacid dimethyl
52313-87-8

3-methyl-2-pentene-1,5-diacid dimethyl

3-methyl-4-p-tolylhydrazono-pentenedioic acid dimethyl ester
109506-29-8

3-methyl-4-p-tolylhydrazono-pentenedioic acid dimethyl ester

3-methyl-2-pentene-1,5-diacid dimethyl
52313-87-8

3-methyl-2-pentene-1,5-diacid dimethyl

3-chlorobenzenediazonium
17333-84-5

3-chlorobenzenediazonium

4-(3-chloro-phenylhydrazono)-3-methyl-pentenedioic acid dimethyl ester
109104-33-8

4-(3-chloro-phenylhydrazono)-3-methyl-pentenedioic acid dimethyl ester

3-methyl-2-pentene-1,5-diacid dimethyl
52313-87-8

3-methyl-2-pentene-1,5-diacid dimethyl

3-bromophenyldiazonium chloride
20893-74-7

3-bromophenyldiazonium chloride

4-(3-bromo-phenylhydrazono)-3-methyl-pentenedioic acid dimethyl ester
109286-51-3

4-(3-bromo-phenylhydrazono)-3-methyl-pentenedioic acid dimethyl ester

3-methyl-2-pentene-1,5-diacid dimethyl
52313-87-8

3-methyl-2-pentene-1,5-diacid dimethyl

3,4-dimethoxy-benzaldehyde
120-14-9

3,4-dimethoxy-benzaldehyde

3-methyl-4-((E)-veratrylidene)-cis-pentenedioic acid
109311-73-1, 136454-20-1

3-methyl-4-((E)-veratrylidene)-cis-pentenedioic acid

Conditions
ConditionsYield
With potassium hydroxide
3-methyl-2-pentene-1,5-diacid dimethyl
52313-87-8

3-methyl-2-pentene-1,5-diacid dimethyl

hexanal
66-25-1

hexanal

4-methyl-6-oxo-2-pentyl-3,6-dihydro-2H-pyran-3-carboxylic acid
108754-34-3

4-methyl-6-oxo-2-pentyl-3,6-dihydro-2H-pyran-3-carboxylic acid

Conditions
ConditionsYield
With potassium hydroxide
3-methyl-2-pentene-1,5-diacid dimethyl
52313-87-8

3-methyl-2-pentene-1,5-diacid dimethyl

meta-hydroxybenzaldehyde
100-83-4

meta-hydroxybenzaldehyde

4-((E)-3-hydroxy-benzylidene)-3-methyl-ξ-pentenedioic acid

4-((E)-3-hydroxy-benzylidene)-3-methyl-ξ-pentenedioic acid

Conditions
ConditionsYield
With potassium hydroxide
3-methyl-2-pentene-1,5-diacid dimethyl
52313-87-8

3-methyl-2-pentene-1,5-diacid dimethyl

(Z)-4-[3,7-Dimethyl-oct-(E)-ylidene]-3-methyl-pent-2-enedioic acid

(Z)-4-[3,7-Dimethyl-oct-(E)-ylidene]-3-methyl-pent-2-enedioic acid

Conditions
ConditionsYield
With sodium hydroxide In methanol
3-methyl-2-pentene-1,5-diacid dimethyl
52313-87-8

3-methyl-2-pentene-1,5-diacid dimethyl

7-methoxy-3,7-dimethyloctanal
3613-30-7

7-methoxy-3,7-dimethyloctanal

(Z)-4-[7-Hydroxy-3,7-dimethyl-oct-(E)-ylidene]-3-methyl-pent-2-enedioic acid
95758-69-3

(Z)-4-[7-Hydroxy-3,7-dimethyl-oct-(E)-ylidene]-3-methyl-pent-2-enedioic acid

Conditions
ConditionsYield
With sodium hydroxide In methanol
3-methyl-2-pentene-1,5-diacid dimethyl
52313-87-8

3-methyl-2-pentene-1,5-diacid dimethyl

7-methoxy-3,7-dimethyloctanal
3613-30-7

7-methoxy-3,7-dimethyloctanal

(Z,E)-(+/-)-4-(7-methoxy-3,7-dimethyloctylidene)-3-methylpent-2-ene-1,5-dioic acid
53023-60-2

(Z,E)-(+/-)-4-(7-methoxy-3,7-dimethyloctylidene)-3-methylpent-2-ene-1,5-dioic acid

Conditions
ConditionsYield
With sodium hydroxide In methanol
3-methyl-2-pentene-1,5-diacid dimethyl
52313-87-8

3-methyl-2-pentene-1,5-diacid dimethyl

(2Z,4E)-3-methyl-5-[2,6,6-trimethylcyclohex-1-enyl]penta-2,4-dienal
54226-17-4

(2Z,4E)-3-methyl-5-[2,6,6-trimethylcyclohex-1-enyl]penta-2,4-dienal

11-cis,13-cis-12-carboxyretinoic acid
81176-73-0

11-cis,13-cis-12-carboxyretinoic acid

Conditions
ConditionsYield
With potassium hydroxide In methanol for 64h; Ambient temperature;

52313-87-8Relevant articles and documents

Method for preparing dimethyl 3-methylpentyl-2-enedionate

-

Paragraph 0027; 0033-0036, (2018/07/30)

The invention provides a method for preparing dimethyl 3-methylpentyl-2-enedionate. The method has the advantages of easy availability of raw materials, high yield and less waste residues, and is suitable for industrial production.

Allosteric effects in binuclear homo- and heterometallic triple-stranded lanthanide podates

Ryan, Patrick E.,Canard, Gabriel,Koeller, Sylvain,Bocquet, Bernard,Piguet, Claude

, p. 10012 - 10024 (2012/10/30)

This work illustrates a simple approach for deciphering and exploiting the various free energy contributions to the global complexation process leading to the binuclear triple-stranded podates [Ln2(L9)]6+ (Ln is a trivalent lanthanide). Despite the larger microscopic affinities exhibited by the binding sites for small Ln3+, the stability constants measured for [Ln2(L9)]6+ decrease along the lanthanide series; a phenomenon which can be ascribed to the severe enthalpic penalty accompanying the intramolecular cyclization around small Ln(III), combined with increasing anticooperative allosteric interligand interactions. Altogether, the microscopic thermodynamic characteristics predict β1,1,1 La,Lu,L9/β1,1,1Lu,La,L9 = 145 for the ratio of the formation constants of the target heterobimetallic [LaLu(L9)] 6+ and [LuLa(L9)]6+ microspecies, a value in line with the quantitative preparation (>90%) of [LaLu(L9)]6+ at millimolar concentrations. Preliminary NMR titrations indeed confirm the rare thermodynamic programming of a pure heterometallic f-f′ complex.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 52313-87-8