CHEMBRDG-BB 4011041

Base Information

Chemical Name:CHEMBRDG-BB 4011041
CAS No.:915921-59-4
Molecular Formula:C₁₀H₁₂N₂O
Molecular Weight:176.218
Hs Code.:
Mol file:915921-59-4.mol

Synonyms:

Suppliers and Price of CHEMBRDG-BB 4011041

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
(4,5-Dimethyl-1H-benzimidazol-2-yl)methanol
500mg
$ 75.00

Matrix Scientific
(6,7-Dimethyl-1H-benzimidazol-2-yl)methanol
500mg
$ 189.00

Crysdot
(6,7-Dimethyl-1H-benzo[d]imidazol-2-yl)methanol 95+%
5g
$ 668.00

ChemBridge Corporation
(6,7-dimethyl-1H-benzimidazol-2-yl)methanol 95%
5 g
$ 133.00

Biosynth Carbosynth
(4,5-Dimethyl-1H-benzimidazol-2-yl)methanol
1 g
$ 105.00

Biosynth Carbosynth
(4,5-Dimethyl-1H-benzimidazol-2-yl)methanol
500 mg
$ 60.00

Biosynth Carbosynth
(4,5-Dimethyl-1H-benzimidazol-2-yl)methanol
2 g
$ 179.00

Biosynth Carbosynth
(4,5-Dimethyl-1H-benzimidazol-2-yl)methanol
5 g
$ 358.00

Biosynth Carbosynth
(4,5-Dimethyl-1H-benzimidazol-2-yl)methanol
10 g
$ 609.00

American Custom Chemicals Corporation
(6,7-DIMETHYL-1H-BENZIMIDAZOL-2-YL)METHANOL 95.00%
1G
$ 646.80

Total 6 raw suppliers

Chemical Property of CHEMBRDG-BB 4011041

Chemical Property:

Vapor Pressure:4.06E-08mmHg at 25°C

Purity/Quality:

97% ^*data from raw suppliers

(4,5-Dimethyl-1H-benzimidazol-2-yl)methanol ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:Xi

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of CHEMBRDG-BB 4011041

There total 1 articles about CHEMBRDG-BB 4011041 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:

: 79-14-1
glycolic Acid

: 41927-01-9
3,4-dimethyl-o-phenylenediamine

: 915921-59-4
C₁₀H₁₂N₂O

Guidance literature:: With hydrogenchloride; In water; for 6h; Reflux;
DOI:10.1016/j.bmcl.2011.12.074

Reference yield:

: 915921-59-4
C₁₀H₁₂N₂O

: 1357162-37-8
C₂₂H₂₂N₂O₃

Guidance literature:: Multi-step reaction with 3 steps

1: tetrabutylammomium bromide; potassium hydroxide / tetrahydrofuran / 0 °C

2: Dess-Martin periodane / dichloromethane / 6 h / 0 °C

3: potassium hydroxide / ethanol / 10 h / Cooling with ice

With tetrabutylammomium bromide; Dess-Martin periodane; potassium hydroxide; In tetrahydrofuran; ethanol; dichloromethane; 2: Dess-Martin oxidation / 3: Aldol condensation;
DOI:10.1016/j.bmcl.2011.12.074

Reference yield:

: 915921-59-4
C₁₀H₁₂N₂O

: 1357162-28-7
C₂₂H₂₂N₂O₃

Guidance literature:: Multi-step reaction with 3 steps

1: tetrabutylammomium bromide; potassium hydroxide / tetrahydrofuran / 0 °C

2: Dess-Martin periodane / dichloromethane / 6 h / 0 °C

3: potassium hydroxide / ethanol / 10 h / Cooling with ice

With tetrabutylammomium bromide; Dess-Martin periodane; potassium hydroxide; In tetrahydrofuran; ethanol; dichloromethane; 2: Dess-Martin oxidation / 3: Aldol condensation;
DOI:10.1016/j.bmcl.2011.12.074