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117903-25-0

BOC-MENLE-OH is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 117903-25-0 Structure

  • Basic information

    1. Product Name: BOC-MENLE-OH
    2. Synonyms: BOC-L-MENLE-OH;BOC-N-ALPHA-METHYL-L-NORLEUCINE;BOC-MENLE-OH;BOC-MEAHX(2)-OH;BOC-MEACPO(2)-OH;BOC-N-ME-NLE-OH;BOC-N-ME-NORLEUCINE;BOC-N-ME-L-2-AMINOHEXANOIC ACID
    3. CAS NO:117903-25-0
    4. Molecular Formula: C12H23NO4
    5. Molecular Weight: 245.32
    6. EINECS: N/A
    7. Product Categories: Amino Acid Derivatives;N-Methyl Amino Acids;amino acids
    8. Mol File: 117903-25-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 343.6 °C at 760 mmHg
    3. Flash Point: 161.6 °C
    4. Appearance: /
    5. Density: 1.055 g/cm3
    6. Vapor Pressure: 1.25E-05mmHg at 25°C
    7. Refractive Index: 1.468
    8. Storage Temp.: Store at 0-5°C
    9. Solubility: N/A
    10. PKA: 4.03±0.21(Predicted)
    11. CAS DataBase Reference: BOC-MENLE-OH(CAS DataBase Reference)
    12. NIST Chemistry Reference: BOC-MENLE-OH(117903-25-0)
    13. EPA Substance Registry System: BOC-MENLE-OH(117903-25-0)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 117903-25-0(Hazardous Substances Data)

117903-25-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 117903-25-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,9,0 and 3 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 117903-25:
(8*1)+(7*1)+(6*7)+(5*9)+(4*0)+(3*3)+(2*2)+(1*5)=120
120 % 10 = 0
So 117903-25-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H23NO4/c1-6-7-8-9(10(14)15)13(5)11(16)17-12(2,3)4/h9H,6-8H2,1-5H3,(H,14,15)/t9-/m0/s1

117903-25-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-2-[methyl-[(2-methylpropan-2-yl)oxycarbonyl]amino]hexanoic acid

1.2 Other means of identification

Product number -
Other names N-Methyl-N-{[(2-methyl-2-propanyl)oxy]carbonyl}-L-norleucine

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:117903-25-0 SDS

117903-25-0Relevant articles and documents

Synthesis of new indolactam analogues by microbial conversion

Kajiyama, Shin-Ichiro,Irie, Kazuhiro,Kido, Takae,Koshimizu, Koichi,Hayashi, Hideo,Arai, Motoo

, p. 5453 - 5462 (2007/10/02)

Ten indolactam congeners with L-Ala, Abu, γ,δ-Δ-Nva, Nva, Nle, tert-Leu, Leu, Ile, allo-Ile. Phg instead ofL-Val in (-)-indolactam-Val, were synthesized from their seco-compounds (N-methyl-L-amino acidyl-L-tryptophonol) by microbial conversion.

Nor-statine and nor-cyclostatine polypeptides

-

, (2008/06/13)

Polypeptides and derivatives thereof containing nor-statine and nor-cyclostatine are useful for inhibiting the angiotensinogen-cleaving action of the enzyme renin.

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