C₃₄H₄₈O₁₃S

Base Information

Chemical Name:C₃₄H₄₈O₁₃S
CAS No.:850656-83-6
Molecular Formula:C₃₄H₄₈O₁₃S
Molecular Weight:696.813
Hs Code.:

C<sub>34</sub>H<sub>48</sub>O<sub>13</sub>S

Synonyms:C₃₄H₄₈O₁₃S

Suppliers and Price of C₃₄H₄₈O₁₃S

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 C₃₄H₄₈O₁₃S

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₃₄H₄₈O₁₃S

There total 40 articles about C₃₄H₄₈O₁₃S 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: 98.0%

: 922-67-8
propynoic acid methyl ester

: 568572-08-7
C₃₀H₄₄O₁₁S

: 850656-83-6
C₃₄H₄₈O₁₃S

Guidance literature:: With 4-methyl-morpholine; In dichloromethane; at 20 ℃;
DOI:10.1021/ja042686r

Reference yield:

: 568572-05-4
C₂₃H₃₄O₈

: 850656-83-6
C₃₄H₄₈O₁₃S

Guidance literature:: Multi-step reaction with 9 steps

1: 88 percent / NaBH₄; CeCl₃*7H₂O / CH₂Cl₂; methanol / 0.5 h / 0 °C

2: 83 percent / NaHCO₃; mCPBA / CH₂Cl₂ / 11.5 h / 20 °C

3: 81 percent / N-methylmorpholine-N-oxide; tetra-n-propylammonium perruthenate; 4A molecular sieves / CH₂Cl₂ / 1 h / 20 °C

4: 100 percent / Na[PhSeB(OEt)3] / ethanol / 0 - 20 °C

5: camphorsulfonic acid / CH₂Cl₂ / 4 h / 20 °C

6: L-Selectride / tetrahydrofuran / 0.75 h / -78 °C

7: 78.8 mg / LiAlH₄ / tetrahydrofuran / 0.67 h / 0 °C

8: 81 percent / Et₃N; DMAP / CH₂Cl₂ / 20 °C

9: 98 percent / N-methylmorpholine / CH₂Cl₂ / 20 °C

With 4-methyl-morpholine; dmap; sodium tetrahydroborate; lithium aluminium tetrahydride; cerium(III) chloride; tetrapropylammonium perruthennate; 4 A molecular sieve; camphor-10-sulfonic acid; L-Selectride; sodium hydrogencarbonate; 4-methylmorpholine N-oxide; sodium phenylseleno(triethyl)borate; triethylamine; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; methanol; ethanol; dichloromethane; 1: Luche reduction;
DOI:10.1021/ja042686r

Reference yield:

: 568571-94-8
C₂₃H₃₆O₈

: 850656-83-6
C₃₄H₄₈O₁₃S

Guidance literature:: Multi-step reaction with 8 steps

1: 83 percent / NaHCO₃; mCPBA / CH₂Cl₂ / 11.5 h / 20 °C

2: 81 percent / N-methylmorpholine-N-oxide; tetra-n-propylammonium perruthenate; 4A molecular sieves / CH₂Cl₂ / 1 h / 20 °C

3: 100 percent / Na[PhSeB(OEt)3] / ethanol / 0 - 20 °C

4: camphorsulfonic acid / CH₂Cl₂ / 4 h / 20 °C

5: L-Selectride / tetrahydrofuran / 0.75 h / -78 °C

6: 78.8 mg / LiAlH₄ / tetrahydrofuran / 0.67 h / 0 °C

7: 81 percent / Et₃N; DMAP / CH₂Cl₂ / 20 °C

8: 98 percent / N-methylmorpholine / CH₂Cl₂ / 20 °C

With 4-methyl-morpholine; dmap; lithium aluminium tetrahydride; tetrapropylammonium perruthennate; 4 A molecular sieve; camphor-10-sulfonic acid; L-Selectride; sodium hydrogencarbonate; 4-methylmorpholine N-oxide; sodium phenylseleno(triethyl)borate; triethylamine; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; ethanol; dichloromethane;
DOI:10.1021/ja042686r