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13820-09-2

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13820-09-2 Usage

Description

1,1,1-Trimethoxypentane, also known as Trimethyl orthovalerate, is a clear colorless liquid with unique chemical properties. It is a versatile compound that serves as a key intermediate in the synthesis of various organic compounds and pharmaceuticals.

Uses

1. Used in Pharmaceutical Synthesis:
1,1,1-Trimethoxypentane is used as a synthetic intermediate for the preparation of 1,2,4-triazolo[1,5-c]pyrimidine derivatives, which are human adenosine A3 receptor ligands. These ligands have potential applications in the development of drugs targeting various diseases and conditions.
2. Used in Organic Chemistry:
1,1,1-Trimethoxypentane is used as a precursor to prepare N-sulfonyl and N-sulfinyl imines and imidates, which are important building blocks in organic chemistry and can be utilized in the synthesis of a wide range of compounds.
3. Used in the Preparation of 9-O-Acyl Derivatives:
1,1,1-Trimethoxypentane is employed in the preparation of various 9-O-acyl derivatives of N-acetyland N-glycoloyl-neuraminic acid. These derivatives have potential applications in the development of new drugs and pharmaceuticals.
4. Used in the Synthesis of Benzimidazolyl-Quinazolinones:
1,1,1-Trimethoxypentane is also used in the synthesis of 2-methyl, 2-ethyl, 2-propyl, and 2-butyl-3-benzimidazolyl-4(3H)-quinazolinones. These compounds have potential applications in various fields, including pharmaceuticals and materials science.
5. Used in Research and Development:
The kinetics of unimolecular gas-phase elimination of 1,1,1-Trimethoxypentane has been investigated, providing valuable insights into its chemical properties and potential applications in various industries.

Synthesis Reference(s)

Journal of the American Chemical Society, 68, p. 1922, 1946 DOI: 10.1021/ja01214a015

Check Digit Verification of cas no

The CAS Registry Mumber 13820-09-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,8,2 and 0 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 13820-09:
(7*1)+(6*3)+(5*8)+(4*2)+(3*0)+(2*0)+(1*9)=82
82 % 10 = 2
So 13820-09-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H18O3/c1-5-6-7-8(9-2,10-3)11-4/h5-7H2,1-4H3

13820-09-2 Well-known Company Product Price

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  • (Code)Product description
  • CAS number
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  • Detail
  • Alfa Aesar

  • (L20377)  Trimethyl orthovalerate, 98%   

  • 13820-09-2

  • 5g

  • 188.0CNY

  • Detail
  • Alfa Aesar

  • (L20377)  Trimethyl orthovalerate, 98%   

  • 13820-09-2

  • 25g

  • 776.0CNY

  • Detail
  • Alfa Aesar

  • (L20377)  Trimethyl orthovalerate, 98%   

  • 13820-09-2

  • 100g

  • 2597.0CNY

  • Detail
  • Sigma-Aldrich

  • (75607)  Trimethylorthovalerate  purum, ≥97.0% (GC)

  • 13820-09-2

  • 75607-10ML

  • 643.50CNY

  • Detail
  • Sigma-Aldrich

  • (75607)  Trimethylorthovalerate  purum, ≥97.0% (GC)

  • 13820-09-2

  • 75607-50ML

  • 2,241.72CNY

  • Detail
  • Aldrich

  • (254517)  Trimethylorthovalerate  97%

  • 13820-09-2

  • 254517-5G

  • 439.92CNY

  • Detail

13820-09-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,1-Trimethoxypentane

1.2 Other means of identification

Product number -
Other names triethyl orthovalerate

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:13820-09-2 SDS

13820-09-2Relevant articles and documents

A flexible Pinner preparation of orthoesters: The model case of trimethylorthobenzoate

Noe, Marco,Perosa, Alvise,Selva, Maurizio

, p. 2252 - 2260 (2013)

In the absence of additional solvents, a novel procedure was implemented for the synthesis of trimethylorthoesters through the Pinner reaction. At 5 °C, the reaction of both aliphatic and aromatic nitriles (RCN; R = Et, Bu, Ph) with a moderate excess of MeOH and gaseous HCl gave the corresponding imidate hydrochlorides [RC(NH)OR′·HCl] in excellent yields (>90%). At 25-65 °C, the methanolysis of alkyl imidate salts provided trimethylortho-propionate and valerate, while only traces of trimethylorthobenzoate (TMOB) were observed. However, the aromatic hydrochloride could be readily converted into the hydrogenphosphate salt [PhC(NH) OR′·H3PO4] which, in turn, underwent a selective (>80%) reaction with MeOH to produce TMOB in a 62% isolated yield. This allowed for an unprecedented Pinner-type synthesis of TMOB starting from benzonitrile, rather than from the highly toxic trichloromethylbenzene. Overall, remarkable improvements in safety and process intensification were achieved.

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