(4R)-1-Methyl-4-propyl-L-proline Hydrochloride

Base Information

Chemical Name:(4R)-1-Methyl-4-propyl-L-proline Hydrochloride
CAS No.:6734-79-8
Molecular Formula:C₉H₁₇NO₂*ClH
Molecular Weight:207.7
Hs Code.:
Mol file:6734-79-8.mol

Synonyms:(4R)-1-Methyl-4-propyl-L-proline Hydrochloride;1-Methyl-4-propyl-L-trans-proline Hydrochloride;4-n-Propyl Hygric Acid Hydrochloride;L-trans-1-Methyl-4-propyl-proline Hydrochloride;trans-Propylhygric Acid Hydrochloride

Suppliers and Price of (4R)-1-Methyl-4-propyl-L-proline Hydrochloride

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
(4R)-1-Methyl-4-propyl-L-prolineHydrochloride
100mg
$ 585.00

American Custom Chemicals Corporation
(4R)-1-METHYL-4-PROPYL-L-PROLINE HYDROCHLORIDE 95.00%
250MG
$ 1871.10

American Custom Chemicals Corporation
(4R)-1-METHYL-4-PROPYL-L-PROLINE HYDROCHLORIDE 95.00%
25MG
$ 739.20

American Custom Chemicals Corporation
(4R)-1-METHYL-4-PROPYL-L-PROLINE HYDROCHLORIDE 95.00%
10MG
$ 349.65

Total 7 raw suppliers

Chemical Property of (4R)-1-Methyl-4-propyl-L-proline Hydrochloride

Chemical Property:

PSA：40.54000
LogP:1.93130
Storage Temp.:Refrigerator
Solubility.:Methanol (Slightly), Water (Slightly, Sonicated)

Purity/Quality:

97% ^*data from raw suppliers

(4R)-1-Methyl-4-propyl-L-prolineHydrochloride ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of (4R)-1-Methyl-4-propyl-L-proline Hydrochloride

There total 7 articles about (4R)-1-Methyl-4-propyl-L-proline Hydrochloride 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:

: 50-00-0,30525-89-4,61233-19-0
formaldehyd

: C₈H₁₅NO₂*ClH

: 6734-79-8
1-methyl-trans-4-propyl-L-proline hydrochloride

Guidance literature:: With palladium on activated carbon; hydrogen; In methanol; water; under 3750.38 Torr;
DOI:10.1039/C9OB00003H

Reference yield:

: C₁₅H₂₁NO₄S

: 6734-79-8
1-methyl-trans-4-propyl-L-proline hydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1.1: sodium; naphthalene / tetrahydrofuran / 2 h / Inert atmosphere; Cooling

1.2: pH 0 - 1

2.1: hydrogen; palladium on activated carbon / methanol; water / 3750.38 Torr

With naphthalene; palladium on activated carbon; hydrogen; sodium; In tetrahydrofuran; methanol; water;
DOI:10.1039/C9OB00003H

Reference yield:

: C₁₇H₂₅NO₃S

: 6734-79-8
1-methyl-trans-4-propyl-L-proline hydrochloride

Guidance literature:: Multi-step reaction with 5 steps

1.1: tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride / toluene / 70 °C / Inert atmosphere

2.1: o-(diphenylphosphino)benzoic acid methyl ether; bis(norbornadiene)rhodium(l)tetrafluoroborate; hydrogen / dichloromethane / 24 h / 20 °C / 5171.62 Torr

3.1: sodium periodate; ruthenium(III) chloride trihydrate / chloroform; water; acetonitrile / 2 h / 20 °C

4.1: sodium; naphthalene / tetrahydrofuran / 2 h / Inert atmosphere; Cooling

4.2: pH 0 - 1

5.1: hydrogen; palladium on activated carbon / methanol; water / 3750.38 Torr

With tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride; bis(norbornadiene)rhodium(l)tetrafluoroborate; sodium periodate; naphthalene; ruthenium(III) chloride trihydrate; palladium on activated carbon; o-(diphenylphosphino)benzoic acid methyl ether; hydrogen; sodium; In tetrahydrofuran; methanol; dichloromethane; chloroform; water; toluene; acetonitrile;
DOI:10.1039/C9OB00003H