7a-Hydroxycholesterol3-Benzoate

Base Information

Chemical Name:7a-Hydroxycholesterol3-Benzoate
CAS No.:40824-59-7
Molecular Formula:C34H50O3
Molecular Weight:506.77
Hs Code.:
Mol file:40824-59-7.mol

Synonyms:(3,7a)-Cholest-5-ene-3,7-diol 3-Benzoate;7a-Hydroxycholesterol3-Benzoate;Cholest-5-ene-3,7a-diol 3-Benzoate;(3β,7α)-Cholest-5-ene-3,7-diol 3-Benzoate;Cholest-5-ene-3β,7α-diol 3-Benzoate

Suppliers and Price of 7a-Hydroxycholesterol3-Benzoate

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

TRC
(3β,7α)-Cholest-5-ene-3,7-diol3-Benzoate
5mg
$ 825.00

TRC
(3β,7α)-Cholest-5-ene-3,7-diol3-Benzoate
2mg
$ 360.00

Biosynth Carbosynth
(3b,7a)-Cholest-5-ene-3,7-diol 3-benzoate
10 mg
$ 1911.00

Biosynth Carbosynth
(3b,7a)-Cholest-5-ene-3,7-diol 3-benzoate
5 mg
$ 1051.10

Biosynth Carbosynth
(3b,7a)-Cholest-5-ene-3,7-diol 3-benzoate
1 mg
$ 318.00

Biosynth Carbosynth
(3b,7a)-Cholest-5-ene-3,7-diol 3-benzoate
2 mg
$ 578.10

American Custom Chemicals Corporation
(3B,7A)-CHOLEST-5-ENE-3,7-DIOL 3-BENZOATE 95.00%
5MG
$ 495.11

Total 3 raw suppliers

Chemical Property of 7a-Hydroxycholesterol3-Benzoate

Chemical Property:

Vapor Pressure:0mmHg at 25°C
Melting Point:160.5-161.5°C
Boiling Point:595.042°C at 760 mmHg
PKA:14.02±0.70(Predicted)
Flash Point:218.194°C
Density:1.08g/cm³
Solubility.:Chloroform, Dichloromethane, Ethyl Acetate

Purity/Quality:

99% ^*data from raw suppliers

(3β,7α)-Cholest-5-ene-3,7-diol3-Benzoate ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses (3β,7α)-Cholest-5-ene-3,7-diol 3-Benzoate (cas# 40824-59-7) is a compound useful in organic synthesis.

Technology Process of 7a-Hydroxycholesterol3-Benzoate

There total 9 articles about 7a-Hydroxycholesterol3-Benzoate 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:

: 6997-41-7
3β-benzoyloxy-cholest-5-en-7-one

: 40824-59-7
3β,7α-cholest-5-ene-3,7-diol-3-benzoate

: 17974-80-0
3β,7β-cholest-5-ene-3,7-diol-3-benzoate

Guidance literature:: With 1,4-dioxane; sodium tetrahydroborate;
DOI:10.1021/ja01521a053

Reference yield:

: 604-32-0
cholesteryl benzoate

: 40824-59-7
3β,7α-cholest-5-ene-3,7-diol-3-benzoate

Guidance literature:: With trithiazyl trichloride; In benzene;

Reference yield:

: 566-28-9
7-Oxocholesterol

: 40824-59-7
3β,7α-cholest-5-ene-3,7-diol-3-benzoate

Guidance literature:: Multi-step reaction with 2 steps

1: Et₃N / CH₂Cl₂ / 0 °C

2: 1) 1M L-Selectride, 2) 6 M aq. NaOH, 30percent H₂O₂ / 1) THF, -78 deg C, 5 h, 2) THF, H₂O, r.t., 1 h

With sodium hydroxide; dihydrogen peroxide; L-Selectride; triethylamine; In dichloromethane;
DOI:10.1016/0039-128X(95)93851-O