Cas no 82962-54-7 (Ethyl 2,2-dimethyl-1,3-dioxane-5-carboxylate)

Ethyl 2,2-dimethyl-1,3-dioxane-5-carboxylate structure
82962-54-7 structure
Product Name:Ethyl 2,2-dimethyl-1,3-dioxane-5-carboxylate
CAS No:82962-54-7
MF:C9H16O4
MW:188.220943450928
MDL:MFCD11975772
CID:1011876
PubChem ID:11019611
Update Time:2024-10-27

Ethyl 2,2-dimethyl-1,3-dioxane-5-carboxylate Chemical and Physical Properties

Names and Identifiers

    • Ethyl 2,2-dimethyl-1,3-dioxane-5-carboxylate
    • 2,2-DIMETHYL-5-CARBETHOXY-1,3-DIOXANE
    • 2,2-diMethyl-5-ethoxycarbonyl-1,3-dioxane
    • 2,2-Dimethyl-[1,3]dioxane-5-carboxylic acid ethyl ester
    • Ethyl 2,2-dimethyl-1,3-dioxane-5-carboxylate (ACI)
    • F12519
    • DB-075889
    • DS-17340
    • MFCD11975772
    • DTXSID40452100
    • EN300-179148
    • 1,3-Dioxane-5-carboxylic acid, 2,2-dimethyl-, ethyl ester
    • SB38910
    • SCHEMBL1867430
    • Ethyl2,2-dimethyl-1,3-dioxane-5-carboxylate
    • 82962-54-7
    • MYGMWHATZAFUIU-UHFFFAOYSA-N
    • SY114002
    • AKOS015918072
    • CS-B1510
    • MDL： MFCD11975772
    • Inchi： 1S/C9H16O4/c1-4-11-8(10)7-5-12-9(2,3)13-6-7/h7H,4-6H2,1-3H3
    • InChI Key： MYGMWHATZAFUIU-UHFFFAOYSA-N
    • SMILES： O=C(C1COC(C)(C)OC1)OCC

Computed Properties

  • Exact Mass: 188.10485899g/mol
  • Monoisotopic Mass: 188.10485899g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 13
  • Rotatable Bond Count: 3
  • Complexity: 178
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 0.6
  • Topological Polar Surface Area: 44.8?2

Experimental Properties

  • Density: 1.039±0.06 g/cm3 (20 oC 760 Torr),
  • Boiling Point: 75 oC (0.4 Torr)
  • Flash Point: 85.0±23.2 oC,
  • Solubility: Slightly soluble (23 g/l) (25 o C),

Ethyl 2,2-dimethyl-1,3-dioxane-5-carboxylate Security Information

Ethyl 2,2-dimethyl-1,3-dioxane-5-carboxylate Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
Alichem
A449038267-10g
Ethyl 2,2-dimethyl-1,3-dioxane-5-carboxylate
 82962-54-7 95%
10g
 $262.15 2023-09-01
Alichem
A449038267-25g
Ethyl 2,2-dimethyl-1,3-dioxane-5-carboxylate
 82962-54-7 95%
25g
 $450.80 2023-09-01
Alichem
A449038267-100g
Ethyl 2,2-dimethyl-1,3-dioxane-5-carboxylate
 82962-54-7 95%
100g
 $1420.00 2023-09-01
Chemenu
CM104951-5g
ethyl 2,2-dimethyl-1,3-dioxane-5-carboxylate
 82962-54-7 95%
5g
 $153 2021-08-06
Chemenu
CM104951-10g
ethyl 2,2-dimethyl-1,3-dioxane-5-carboxylate
 82962-54-7 95%
10g
 $230 2021-08-06
Chemenu
CM104951-25g
ethyl 2,2-dimethyl-1,3-dioxane-5-carboxylate
 82962-54-7 95%
25g
 $430 2021-08-06
Ambeed
A187179-250mg
Ethyl 2,2-dimethyl-1,3-dioxane-5-carboxylate
 82962-54-7 95%
250mg
 $13.0 2025-04-16
Ambeed
A187179-1g
Ethyl 2,2-dimethyl-1,3-dioxane-5-carboxylate
 82962-54-7 95%
1g
 $19.0 2025-04-16
Ambeed
A187179-5g
Ethyl 2,2-dimethyl-1,3-dioxane-5-carboxylate
 82962-54-7 95%
5g
 $39.0 2025-04-16
Ambeed
A187179-10g
Ethyl 2,2-dimethyl-1,3-dioxane-5-carboxylate
 82962-54-7 95%
10g
 $62.0 2025-04-16

Ethyl 2,2-dimethyl-1,3-dioxane-5-carboxylate Production Method

Production Method 1

Reaction Conditions
1.1 Reagents: Sodium chloride Solvents: Dimethyl sulfoxide ,  Water ;  20 h, reflux
Reference
Synthesis of Panal Terpenoid Core
Baranov, Mikhail S.; et al, Synlett, 2017, 28(5), 583-588

Production Method 2

Reaction Conditions
1.1 Reagents: Sodium chloride Solvents: Dimethyl sulfoxide ,  Water ;  9 h, reflux
Reference
Design and synthesis of bis 1-thiogalactopyranoside having a cyano group at the aglycon terminal
Zhang, Guoyao; et al, Huaxi Yaoxue Zazhi, 2005, 20(6), 474-476

Production Method 3

Reaction Conditions
1.1 Reagents: Sulfuric acid Solvents: Acetone
1.2 Reagents: Sodium chloride ,  Water Solvents: Dimethyl sulfoxide ;  190 - 195 °C
Reference
Bifunctional acyclic nucleoside phosphonates: 2. Symmetrical 2-{[bis(phosphono)methoxy]methyl}ethyl derivatives of purines and pyrimidines
Vrbkova, Silvie; et al, Collection of Czechoslovak Chemical Communications, 2007, 72(7), 965-983

Production Method 4

Reaction Conditions
1.1 Catalysts: p-Toluenesulfonic acid
1.2 Reagents: Sodium chloride Solvents: Dimethyl sulfoxide
Reference
3,5-Disubstituted pyranone analogues of highly antifungally active furanones: Conversion of biological effect from antifungal to cytostatic
Schiller, Radan; et al, Bioorganic & Medicinal Chemistry Letters, 2010, 20(24), 7358-7360

Production Method 5

Reaction Conditions
1.1 Reagents: Sodium chloride Solvents: Dimethyl sulfoxide
Reference
Synthesis of 5,5'-dihydroxyleucine and 4-fluoro-5,5'-dihydroxyleucine, the reduction products of 4-carboxyglutamic and 4-carboxy-4-fluoroglutamic acids
Dubois, Joelle; et al, Tetrahedron, 1991, 47(6), 1001-12

Production Method 6

Reaction Conditions
1.1 Catalysts: Sodium chloride Solvents: Dimethyl sulfoxide
Reference
Synthesis of 2,2-dimethyl-5-hydroxymethyl-1,3-dioxane
Li, Peijie; et al, Huaxi Yaoxue Zazhi, 2001, 16(4),

Production Method 7

Reaction Conditions
Reference
Synthesis and evaluation of phospholipid analogs as inhibitors of cobra venom phospholipase A2
Yuan, Wei; et al, Journal of the American Chemical Society, 1987, 109(26), 8071-81

Production Method 8

Reaction Conditions
1.1 Reagents: 2,2-Dimethoxypropane ,  p-Toluenesulfonic acid
1.2 Reagents: Sodium chloride Solvents: Dimethyl sulfoxide ,  Water
Reference
Asymmetric functionalization at a prochiral carbon center by the aid of sulfinyl chirality: a selective formation of 6-substituted (3R,SS)- and (3S,SS)-3-(hydroxymethyl)-3,4-dihydro-5-(p-tolyl)sulfinyl-2H-pyrans
Iwata, Chuzo; et al, Tetrahedron Letters, 1987, 28(27), 3131-4

Production Method 9

Reaction Conditions
1.1 Reagents: Benzene Catalysts: p-Toluenesulfonic acid
2.1 -
Reference
Synthesis and evaluation of phospholipid analogs as inhibitors of cobra venom phospholipase A2
Yuan, Wei; et al, Journal of the American Chemical Society, 1987, 109(26), 8071-81

Production Method 10

Reaction Conditions
1.1 Reagents: Sodium bicarbonate Solvents: Water ;  20 °C; 2 h, rt
1.2 Reagents: Triethyl orthoformate Catalysts: p-Toluenesulfonic acid Solvents: Acetone ;  2 h, reflux; reflux → rt
1.3 Reagents: Potassium carbonate ;  neutralized, rt
2.1 Reagents: Sodium chloride Solvents: Dimethyl sulfoxide ,  Water ;  20 h, reflux
Reference
Synthesis of Panal Terpenoid Core
Baranov, Mikhail S.; et al, Synlett, 2017, 28(5), 583-588

Production Method 11

Reaction Conditions
1.1 Reagents: Triethyl orthoformate Catalysts: p-Toluenesulfonic acid Solvents: Acetone ;  2 h, reflux; reflux → rt
1.2 Reagents: Potassium carbonate ;  neutralized, rt
2.1 Reagents: Sodium chloride Solvents: Dimethyl sulfoxide ,  Water ;  20 h, reflux
Reference
Synthesis of Panal Terpenoid Core
Baranov, Mikhail S.; et al, Synlett, 2017, 28(5), 583-588

Production Method 12

Reaction Conditions
1.1 Reagents: Sodium bicarbonate Solvents: Water ;  20 °C; 2 h, rt
2.1 Reagents: Triethyl orthoformate Catalysts: p-Toluenesulfonic acid Solvents: Acetone ;  2 h, reflux; reflux → rt
2.2 Reagents: Potassium carbonate ;  neutralized, rt
3.1 Reagents: Sodium chloride Solvents: Dimethyl sulfoxide ,  Water ;  20 h, reflux
Reference
Synthesis of Panal Terpenoid Core
Baranov, Mikhail S.; et al, Synlett, 2017, 28(5), 583-588

Production Method 13

Reaction Conditions
1.1 Reagents: p-Toluenesulfonic acid Solvents: Acetone
2.1 Reagents: Sodium chloride Solvents: Dimethyl sulfoxide
Reference
Synthesis of 5,5'-dihydroxyleucine and 4-fluoro-5,5'-dihydroxyleucine, the reduction products of 4-carboxyglutamic and 4-carboxy-4-fluoroglutamic acids
Dubois, Joelle; et al, Tetrahedron, 1991, 47(6), 1001-12

Production Method 14

Reaction Conditions
1.1 Reagents: Potassium bicarbonate Solvents: Methanol ,  Water
2.1 Reagents: p-Toluenesulfonic acid Solvents: Acetone
3.1 Reagents: Sodium chloride Solvents: Dimethyl sulfoxide
Reference
Synthesis of 5,5'-dihydroxyleucine and 4-fluoro-5,5'-dihydroxyleucine, the reduction products of 4-carboxyglutamic and 4-carboxy-4-fluoroglutamic acids
Dubois, Joelle; et al, Tetrahedron, 1991, 47(6), 1001-12

Ethyl 2,2-dimethyl-1,3-dioxane-5-carboxylate Raw materials

Ethyl 2,2-dimethyl-1,3-dioxane-5-carboxylate Preparation Products

Ethyl 2,2-dimethyl-1,3-dioxane-5-carboxylate Related Literature

Related Categories

82962-54-7 (Ethyl 2,2-dimethyl-1,3-dioxane-5-carboxylate) Related Products

Recommended suppliers
鉅瀾化工科技(青島)有限公司
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
鉅瀾化工科技(青島)有限公司
SunaTech Inc.
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Reagent
SunaTech Inc.
Tiancheng Chemical (Jiangsu) Co., Ltd
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Inner Mongolia Xinhong Biological Technology Co., Ltd
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Inner Mongolia Xinhong Biological Technology Co., Ltd
Shenzhen Jianxing Pharmaceutical Technology Co., Ltd.
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Reagent
Shenzhen Jianxing Pharmaceutical Technology Co., Ltd.