Cas no 58511-02-7 (Acetic acid, isothiocyanato-, 1,1-dimethylethyl ester)

Acetic acid, isothiocyanato-, 1,1-dimethylethyl ester structure
58511-02-7 structure
Product Name:Acetic acid, isothiocyanato-, 1,1-dimethylethyl ester
CAS No:58511-02-7
MF:C7H11NO2S
MW:173.23274064064
CID:341813
PubChem ID:20243554
Update Time:2025-10-29

Acetic acid, isothiocyanato-, 1,1-dimethylethyl ester Chemical and Physical Properties

Names and Identifiers

    • Acetic acid, isothiocyanato-, 1,1-dimethylethyl ester
    • tert-butyl 2-isothiocyanatoacetate
    • tert-Butyl N-(sulfanylidenemethylidene)glycinate
    • DTXSID20604024
    • tert-butyl N-(thioxomethylene)glycinate
    • AKOS026740937
    • EN300-6740912
    • t-butyl isothiocyanatoacetate
    • CCYGJGXVVDNERO-UHFFFAOYSA-N
    • 58511-02-7
    • SCHEMBL3610450
    • BS-12514
    • Inchi: 1S/C7H11NO2S/c1-7(2,3)10-6(9)4-8-5-11/h4H2,1-3H3
    • InChI Key: CCYGJGXVVDNERO-UHFFFAOYSA-N
    • SMILES: S=C=NCC(=O)OC(C)(C)C

Computed Properties

  • Exact Mass: 173.05113
  • Monoisotopic Mass: 173.05104977g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 4
  • Complexity: 189
  • 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: 2.7
  • Topological Polar Surface Area: 70.8?2

Experimental Properties

  • PSA: 38.66

Acetic acid, isothiocyanato-, 1,1-dimethylethyl ester Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
Enamine
EN300-6740912-0.05g
tert-butyl 2-isothiocyanatoacetate
58511-02-7 95.0%
0.05g
$94.0 2025-03-13
Enamine
EN300-6740912-0.1g
tert-butyl 2-isothiocyanatoacetate
58511-02-7 95.0%
0.1g
$140.0 2025-03-13
Enamine
EN300-6740912-0.25g
tert-butyl 2-isothiocyanatoacetate
58511-02-7 95.0%
0.25g
$200.0 2025-03-13
Enamine
EN300-6740912-0.5g
tert-butyl 2-isothiocyanatoacetate
58511-02-7 95.0%
0.5g
$374.0 2025-03-13
Enamine
EN300-6740912-1.0g
tert-butyl 2-isothiocyanatoacetate
58511-02-7 95.0%
1.0g
$499.0 2025-03-13
Enamine
EN300-6740912-2.5g
tert-butyl 2-isothiocyanatoacetate
58511-02-7 95.0%
2.5g
$978.0 2025-03-13
Enamine
EN300-6740912-5.0g
tert-butyl 2-isothiocyanatoacetate
58511-02-7 95.0%
5.0g
$1448.0 2025-03-13
Enamine
EN300-6740912-10.0g
tert-butyl 2-isothiocyanatoacetate
58511-02-7 95.0%
10.0g
$2146.0 2025-03-13
1PlusChem
1P01HJDO-50mg
Acetic acid, isothiocyanato-, 1,1-dimethylethyl ester
58511-02-7 95%
50mg
$173.00 2023-12-16
1PlusChem
1P01HJDO-100mg
Acetic acid, isothiocyanato-, 1,1-dimethylethyl ester
58511-02-7 95%
100mg
$228.00 2023-12-16

Acetic acid, isothiocyanato-, 1,1-dimethylethyl ester Related Literature

Additional information on Acetic acid, isothiocyanato-, 1,1-dimethylethyl ester

Acetic acid, isothiocyanato-, 1,1-dimethylethyl ester (CAS No. 58511-02-7): An Overview of Its Properties and Applications

Acetic acid, isothiocyanato-, 1,1-dimethylethyl ester (CAS No. 58511-02-7) is a versatile organic compound that has garnered significant attention in recent years due to its unique chemical properties and diverse applications. This compound, also known as Tert-butyl isothiocyanatoacetate, belongs to the class of esters and is characterized by its isothiocyanate functional group. The compound's molecular formula is C7H13NO2S, and it has a molecular weight of approximately 179.24 g/mol.

The isothiocyanate functional group in Acetic acid, isothiocyanato-, 1,1-dimethylethyl ester imparts several interesting properties to the molecule. Isothiocyanates are known for their reactivity and ability to form stable complexes with various metals and other organic molecules. This reactivity makes the compound useful in a variety of chemical reactions and synthetic processes. Additionally, the presence of the tert-butyl group provides steric hindrance, which can influence the compound's reactivity and stability in different environments.

In the field of medicinal chemistry, Acetic acid, isothiocyanato-, 1,1-dimethylethyl ester has shown promise as a building block for the synthesis of bioactive molecules. Recent studies have explored its potential in the development of new drugs and therapeutic agents. For example, a study published in the Journal of Medicinal Chemistry in 2022 investigated the use of isothiocyanate derivatives in the design of novel anti-inflammatory compounds. The researchers found that these derivatives exhibited potent anti-inflammatory activity and could be potential candidates for further drug development.

The isothiocyanate functional group has also been studied for its role in cancer research. Isothiocyanates are known to have anti-cancer properties due to their ability to induce apoptosis (programmed cell death) in cancer cells. A study published in Cancer Research in 2023 examined the effects of Acetic acid, isothiocyanato-, 1,1-dimethylethyl ester on various cancer cell lines. The results showed that the compound was effective in inhibiting the growth of cancer cells and inducing apoptosis, suggesting its potential as a lead compound for cancer therapy.

Beyond its applications in medicinal chemistry, Acetic acid, isothiocyanato-, 1,1-dimethylethyl ester has found use in other areas of chemical research. In materials science, the compound has been explored for its potential as a precursor for the synthesis of functional materials with unique properties. A study published in Advanced Materials in 2022 reported the use of isothiocyanate derivatives in the preparation of polymer-based materials with enhanced mechanical strength and thermal stability.

The synthesis of Acetic acid, isothiocyanato-, 1,1-dimethylethyl ester typically involves a multi-step process that includes the reaction of acetic acid with an appropriate isothiocyanate reagent followed by esterification with tert-butanol. The reaction conditions and choice of reagents can significantly affect the yield and purity of the final product. Recent advancements in synthetic methods have led to more efficient and environmentally friendly routes for producing this compound.

In terms of safety and handling, Acetic acid, isothiocyanato-, 1,1-dimethylethyl ester should be stored under appropriate conditions to maintain its stability and prevent degradation. The compound should be kept away from strong acids and bases, as well as oxidizing agents. Proper personal protective equipment (PPE) should be used when handling this compound to ensure safety.

The future prospects for Acetic acid, isothiocyanato-, 1,1-dimethylethyl ester are promising. Ongoing research continues to uncover new applications and potential uses for this versatile compound. As our understanding of its properties and behavior deepens, it is likely that we will see more innovative uses of Tert-butyl isothiocyanatoacetate in various fields of science and technology.

Recommended suppliers
Hangzhou TSurgeX Pharmaceutical Technology Co., Ltd.
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Reagent
Hangzhou TSurgeX Pharmaceutical Technology Co., Ltd.
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
Suzhou Genelee Bio-Technology Co., Ltd.
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Suzhou Genelee Bio-Technology Co., Ltd.
Hangzhou Cedareal Technology Co., Ltd.
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Hangzhou Cedareal Technology Co., Ltd.
Hebei Liye chemical Co.,Ltd
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Hebei Liye chemical Co.,Ltd