C₃₀H₃₅ClO₅

Base Information

Chemical Name:C₃₀H₃₅ClO₅
CAS No.:594855-20-6
Molecular Formula:C₃₀H₃₅ClO₅
Molecular Weight:511.058
Hs Code.:

C<sub>30</sub>H<sub>35</sub>ClO<sub>5</sub>

Synonyms:

Suppliers and Price of C₃₀H₃₅ClO₅

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 C₃₀H₃₅ClO₅

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₃₀H₃₅ClO₅

There total 16 articles about C₃₀H₃₅ClO₅ 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:

: 487-68-3
mesytaldehyde

: 594855-20-6
C₃₀H₃₅ClO₅

Guidance literature:: Multi-step reaction with 6 steps

1.1: camphorsulfonic acid; 4A molecular sieves; MgSO₄ / CHCl₃

2.1: lithium hexamethyldisilazide; HMPA / tetrahydrofuran

2.2: 57 percent / HMPA / tetrahydrofuran

3.1: tetrabutylammonium fluoride / tetrahydrofuran

4.1: benzene; methanol

5.1: 88 percent / DMAP; pyridine

6.1: 74 percent / lithium hexamethyldisilazide; HMPA / 1,2-dimethoxy-ethane

With pyridine; N,N,N,N,N,N-hexamethylphosphoric triamide; dmap; 4 A molecular sieve; camphor-10-sulfonic acid; tetrabutyl ammonium fluoride; magnesium sulfate; lithium hexamethyldisilazane; In tetrahydrofuran; methanol; 1,2-dimethoxyethane; chloroform; benzene; 6.1: Dieckmann condensation;
DOI:10.1248/cpb.52.163

Reference yield:

: 224622-38-2
(S)-1-(3'-bromophenyl)-1-propanol

: 594855-20-6
C₃₀H₃₅ClO₅

Guidance literature:: Multi-step reaction with 15 steps

1.1: n-BuLi / tetrahydrofuran

1.2: 100 percent / tetrahydrofuran

2.1: 61 percent / imidazole / dimethylformamide

3.1: 92 percent / NaBH₄ / ethanol

4.1: 95 percent / NaH / tetrahydrofuran

5.1: 94 percent / n-Bu₃SnH / toluene

6.1: 70 percent / aq. p-TsOH / ethanol

7.1: 96 percent / (COCl)2; DMSO; TEA / CH₂Cl₂

8.1: 29 percent / NaH; N-chlorosuccinimide / tetrahydrofuran

9.1: 89 percent / DIBAL-H / CH₂Cl₂

10.1: 77 percent / I₂; Ph₃P; imidazole / diethyl ether; acetonitrile

11.1: lithium hexamethyldisilazide; HMPA / tetrahydrofuran

11.2: 57 percent / HMPA / tetrahydrofuran

12.1: tetrabutylammonium fluoride / tetrahydrofuran

13.1: benzene; methanol

14.1: 88 percent / DMAP; pyridine

15.1: 74 percent / lithium hexamethyldisilazide; HMPA / 1,2-dimethoxy-ethane

With pyridine; 1H-imidazole; N,N,N,N,N,N-hexamethylphosphoric triamide; dmap; sodium tetrahydroborate; N-chloro-succinimide; n-butyllithium; oxalyl dichloride; TEA; tetrabutyl ammonium fluoride; iodine; tri-n-butyl-tin hydride; sodium hydride; diisobutylaluminium hydride; toluene-4-sulfonic acid; dimethyl sulfoxide; triphenylphosphine; lithium hexamethyldisilazane; In tetrahydrofuran; methanol; 1,2-dimethoxyethane; diethyl ether; ethanol; dichloromethane; N,N-dimethyl-formamide; toluene; acetonitrile; benzene; 7.1: Swern oxidation / 15.1: Dieckmann condensation;
DOI:10.1248/cpb.52.163

Reference yield:

: (S)-2-(2,4,6-Trimethyl-phenyl)-[1,3]dioxolane-4-carboxylic acid methyl ester

: 594855-20-6
C₃₀H₃₅ClO₅

Guidance literature:: Multi-step reaction with 5 steps

1.1: lithium hexamethyldisilazide; HMPA / tetrahydrofuran

1.2: 57 percent / HMPA / tetrahydrofuran

2.1: tetrabutylammonium fluoride / tetrahydrofuran

3.1: benzene; methanol

4.1: 88 percent / DMAP; pyridine

5.1: 74 percent / lithium hexamethyldisilazide; HMPA / 1,2-dimethoxy-ethane

With pyridine; N,N,N,N,N,N-hexamethylphosphoric triamide; dmap; tetrabutyl ammonium fluoride; lithium hexamethyldisilazane; In tetrahydrofuran; methanol; 1,2-dimethoxyethane; benzene; 5.1: Dieckmann condensation;
DOI:10.1248/cpb.52.163