Cas 1387007-54-6,(R)-6-(3,4-dimethoxyphenyl)-3-methyl-1-(1-methyl-1H-4,5,6,7-tetrahydrobenzimidazol-2-yl)-1-hexanone

1387007-54-6

Post Buying Request

Basic information

Product Name: (R)-6-(3,4-dimethoxyphenyl)-3-methyl-1-(1-methyl-1H-4,5,6,7-tetrahydrobenzimidazol-2-yl)-1-hexanone
Synonyms:
CAS NO:1387007-54-6
Molecular Formula:
Molecular Weight: 384.519
EINECS: N/A
Product Categories: N/A
Mol File: 1387007-54-6.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (R)-6-(3,4-dimethoxyphenyl)-3-methyl-1-(1-methyl-1H-4,5,6,7-tetrahydrobenzimidazol-2-yl)-1-hexanone(CAS DataBase Reference)
NIST Chemistry Reference: (R)-6-(3,4-dimethoxyphenyl)-3-methyl-1-(1-methyl-1H-4,5,6,7-tetrahydrobenzimidazol-2-yl)-1-hexanone(1387007-54-6)
EPA Substance Registry System: (R)-6-(3,4-dimethoxyphenyl)-3-methyl-1-(1-methyl-1H-4,5,6,7-tetrahydrobenzimidazol-2-yl)-1-hexanone(1387007-54-6)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1387007-54-6(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

1387007-54-6 Suppliers

Recommended suppliersmore

1387007-54-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1387007-54-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,7,0,0 and 7 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1387007-54:
(9*1)+(8*3)+(7*8)+(6*7)+(5*0)+(4*0)+(3*7)+(2*5)+(1*4)=166
166 % 10 = 6
So 1387007-54-6 is a valid CAS Registry Number.

1387007-54-6Upstream product

1387007-54-6Downstream Products

1387007-54-6Relevant articles and documents

Enantioselective conjugate addition of alkylboranes catalyzed by a copper- N-heterocyclic carbene complex

Yoshida, Mika,Ohmiya, Hirohisa,Sawamura, Masaya

, p. 11896 - 11899 (2012/09/07)

The first catalytic enantioselective conjugate addition of alkylboron compounds has been achieved. Reactions between alkylboranes and imidazol-2-yl α,β-unsaturated ketones proceeded with high enantioselectivity under the influence of a Cu(I) catalyst syst

Post a RFQ

Cas No.:

Product Name:

Quantity:

Email:

Company name:

Valid Period:

Detailed Requirements:

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

What can I do for you?
Get Best Price

Get Best Price for 1387007-54-6