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1H-1,4-Diazepine-1-carboxylic acid, hexahydro-5-Methyl-, phenylMethyl ester, (5R)is a complex organic compound belonging to the diazepines family. It features a seven-membered ring with two nitrogen atoms, a carboxylic acid group, a hexahydro-5-methyl group indicating a fully saturated six-membered ring with a methyl group, and a phenylMethyl ester group, which is an ester functional group connected to a phenyl group. The (5R)in its name signifies a specific enantiomer or spatial arrangement of the molecule, contributing to its unique properties.

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  • (5R)-Hexahydro-5-methyl-1H-1,4-diazepine-1-carboxylic acid phenylmethyl ester

    Cas No: 1001401-60-0

  • USD $ 1.2-5.0 / Kiloliter

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  • 1001401-60-0 Structure
  • Basic information

    1. Product Name: 1H-1,4-Diazepine-1-carboxylic acid, hexahydro-5-Methyl-, phenylMethyl ester, (5R)-
    2. Synonyms: 1H-1,4-Diazepine-1-carboxylic acid, hexahydro-5-Methyl-, phenylMethyl ester, (5R)-;Suvorexant InterMediate;(5R)-1H-1,4-Diazepine-1-carboxylic acid, hexahydro-5-Methyl-,phenylMethyl ester;(R)-Benzyl 5-methyl-1,4-diazepane-1-carboxylate/Suvorexant intermediate;New Intermediates;(5R)-Hexahydro-5-methyl-1H-1,4-diazepine-1-carboxylic acid phenylmethyl ester;Benzyl (5R)-5-methyl-1,4-diazepane-1-carboxylate;Benzyl(R)-5-methyl-1,4-diazepane-1-carboxylate
    3. CAS NO:1001401-60-0
    4. Molecular Formula: C14H20N2O2
    5. Molecular Weight: 248.3208
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1001401-60-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
    8. Solubility: N/A
    9. CAS DataBase Reference: 1H-1,4-Diazepine-1-carboxylic acid, hexahydro-5-Methyl-, phenylMethyl ester, (5R)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1H-1,4-Diazepine-1-carboxylic acid, hexahydro-5-Methyl-, phenylMethyl ester, (5R)-(1001401-60-0)
    11. EPA Substance Registry System: 1H-1,4-Diazepine-1-carboxylic acid, hexahydro-5-Methyl-, phenylMethyl ester, (5R)-(1001401-60-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1001401-60-0(Hazardous Substances Data)

1001401-60-0 Usage

Uses

Used in Pharmaceutical Industry:
1H-1,4-Diazepine-1-carboxylic acid, hexahydro-5-Methyl-, phenylMethyl ester, (5R)is used as a pharmaceutical compound for its potential therapeutic applications. Its complex carbon-nitrogen ring structure and various functional groups may contribute to its interaction with biological targets, making it a candidate for the development of new drugs.
Used in Chemical Research:
1H-1,4-Diazepine-1-carboxylic acid, hexahydro-5-Methyl-, phenylMethyl ester, (5R)is used as a research chemical for studying the properties and behavior of diazepines and their derivatives. Its unique structure and enantiomerism provide opportunities for investigating the effects of stereochemistry on chemical reactivity and biological activity.
Used in Drug Synthesis:
1H-1,4-Diazepine-1-carboxylic acid, hexahydro-5-Methyl-, phenylMethyl ester, (5R)is used as an intermediate in the synthesis of other pharmaceutical compounds. Its versatile structure allows for further chemical modifications, making it a valuable building block in the development of new drugs with improved efficacy and reduced side effects.

Check Digit Verification of cas no

The CAS Registry Mumber 1001401-60-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,1,4,0 and 1 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1001401-60:
(9*1)+(8*0)+(7*0)+(6*1)+(5*4)+(4*0)+(3*1)+(2*6)+(1*0)=50
50 % 10 = 0
So 1001401-60-0 is a valid CAS Registry Number.

1001401-60-0SDS

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 (R)-benzyl 5-methyl-1,4-diazepane-1-carboxylate

1.2 Other means of identification

Product number -
Other names (R)-benzyl 5-methyl-1,4-diazepane-1-carboxylate

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:1001401-60-0 SDS

1001401-60-0Downstream Products

1001401-60-0Relevant articles and documents

PROCESS FOR THE RESOLUTION OF (R,S)-DIAZEPANE AND DIAZEPANONE DERIVATIVES

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, (2016/04/05)

The present invention relates to a process for the preparation of an acid salt (T) of a compound of formula (A) (A) as well as to the acid salt (T) and the compound (A) as such,wherein R1 is selected from the group consisting of H, PG1 and RA, with RA being or and wherein PG1 is a suitable protecting group, and wherein n is 0 or 1, wherein the acid salt (T) is the salt of one stereoisomer of a chiral acid, preferably wherein the chiral acid salt is a tartaric acid derivative salt, preferably wherein the tartaric acid derivative salt is selected from the group consisting of 2,3-ditoluoyl tartaric acid salt, 2,3-dibenzoyl tartaric acid salt, 2,3-dianisoyl tartaric acid salt, 2,3-dibenzoyl tartaric acid mono(dimethylamide) salt and a mixture of two or more thereof. Further the present invention relates to use of (T) and/or (A) for the preparation of suvorexant.

NOVEL ROUTES OF SYNTHESIS FOR THE PREPARATION OF SUVOREXANT

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Page/Page column 133; 135, (2016/04/26)

The present invention relates to a process for the preparation of a compound of formula (A), Further, the present invention relates to the respective compound (A) as such and to its use in the preparation of antifungal agent.

SUBSTITUTED DIAZEPAN OREXIN RECEPTOR ANTAGONISTS

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Page/Page column 33, (2008/06/13)

The present invention is directed to substituted diazepan compounds which are antagonists of orexin receptors, and which are useful in the treatment or prevention of neurological and psychiatric disorders and diseases in which orexin receptors are involved. The invention is also directed to pharmaceutical compositions comprising these compounds and the use of these compounds and compositions in the prevention or treatment of such diseases in which orexin receptors are involved.

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