C₁₆H₂₁ClO₄

Base Information

Chemical Name:C₁₆H₂₁ClO₄
CAS No.:1337981-60-8
Molecular Formula:C₁₆H₂₁ClO₄
Molecular Weight:312.793
Hs Code.:

C<sub>16</sub>H<sub>21</sub>ClO<sub>4</sub>

Synonyms:C₁₆H₂₁ClO₄

Suppliers and Price of C₁₆H₂₁ClO₄

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of C₁₆H₂₁ClO₄

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₁₆H₂₁ClO₄

There total 5 articles about C₁₆H₂₁ClO₄ which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 1337981-58-4
C₁₆H₂₃ClO₄

: 1337981-60-8
C₁₆H₂₁ClO₄

Guidance literature:: With sodium hypochlorite; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; tetrabutylammomium bromide; sodium hydrogencarbonate; potassium bromide; In hexane; at -10 - 20 ℃;

Reference yield:

: 197899-19-7
(2R)-1-chloro-2-hydroxy-4-pentene

: 1337981-60-8
C₁₆H₂₁ClO₄

Guidance literature:: Multi-step reaction with 5 steps

1: sodium cyanide / water / 30 - 45 °C

2: hydrogenchloride / 20 °C

3: 1H-imidazole / dichloromethane / 25 - 30 °C

4: N-chloro-succinimide / acetone / 0 - 35 °C

5: sodium hydrogencarbonate; sodium hypochlorite; tetrabutylammomium bromide; potassium bromide; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical / hexane / -10 - 20 °C

With 1H-imidazole; hydrogenchloride; sodium cyanide; sodium hypochlorite; N-chloro-succinimide; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; tetrabutylammomium bromide; sodium hydrogencarbonate; potassium bromide; In hexane; dichloromethane; water; acetone;

Reference yield:

: 181272-46-8
(2R)-1-cyano-2-hydroxy-4-pentene

: 1337981-60-8
C₁₆H₂₁ClO₄

Guidance literature:: Multi-step reaction with 4 steps

1: hydrogenchloride / 20 °C

2: 1H-imidazole / dichloromethane / 25 - 30 °C

3: N-chloro-succinimide / acetone / 0 - 35 °C

4: sodium hydrogencarbonate; sodium hypochlorite; tetrabutylammomium bromide; potassium bromide; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical / hexane / -10 - 20 °C

With 1H-imidazole; hydrogenchloride; sodium hypochlorite; N-chloro-succinimide; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; tetrabutylammomium bromide; sodium hydrogencarbonate; potassium bromide; In hexane; dichloromethane; acetone;