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7-(benzoylamino)heptanoic acid is a chemical compound with the molecular formula C14H17NO3. It is a derivative of heptanoic acid, where the carboxylic acid group is replaced by a benzoylamino group. 7-(benzoylamino)heptanoic acid is an organic molecule that can be found in various pharmaceuticals and chemical research applications. It is characterized by its long-chain structure and the presence of an amide linkage between the benzene ring and the heptanoic acid backbone. The compound's properties, such as solubility and reactivity, can be influenced by the presence of this amide group, making it a versatile building block in the synthesis of more complex molecules.

1149-15-1

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1149-15-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1149-15-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,4 and 9 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1149-15:
(6*1)+(5*1)+(4*4)+(3*9)+(2*1)+(1*5)=61
61 % 10 = 1
So 1149-15-1 is a valid CAS Registry Number.

1149-15-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-(benzoylamino)heptanoic acid

1.2 Other means of identification

Product number -
Other names 7-benzoylamino-heptanoic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1149-15-1 SDS

1149-15-1Relevant academic research and scientific papers

The [(Cp)M(CO)3] (M=Re, 99mTc) building block for imaging agents and bioinorganic probes: Perspectives and limitations

Can, Daniel,Peindy N'Dongo, Harmel W.,Spingler, Bernhard,Schmutz, Paul,Alberto, Roger,Raposinho, Paula,Santos, Isabel

, p. 1849 - 1866,18 (2020/08/24)

Starting from asymmetric Thiele's acid derivatives, two different imaging probes [99mTc(CO)3(CpR)] (R=potential targeting vector) are generated simultaneously in one-pot and from one substrate. This extends the previously introduced

Inhibitors of human histone deacetylase: Synthesis and enzyme and cellular activity of straight chain hydroxamates

Remiszewski, Stacy W.,Sambucetti, Lidia C.,Atadja, Peter,Bair, Kenneth W.,Cornell, Wendy D.,Green, Michael A.,Howell, Kobporn Lulu,Jung, Manfred,Kwon, Paul,Trogani, Nancy,Walker, Heather

, p. 753 - 757 (2007/10/03)

Inhibitors of histone deacetylase (HDAC) have been shown to induce terminal differentiation of human tumor cell lines and to have antitumor effects in vivo. We have prepared analogues of suberoylanilide hydroxamic acid (SAHA) and trichostatin A and have evaluated them in a human HDAC enzyme inhibition assay, a p21waf1 (p21) promoter assay, and in monolayer growth inhibition assays. One compound, 4-(dimethylamino)-N-[7-(hydroxyamino)-7-oxoheptyl]-benzamide, was found to affect the growth of a panel of eight human tumor cell lines differentially.

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