Welcome to LookChem.com Sign In|Join Free

CAS

  • or

888725-91-5

Post Buying Request

888725-91-5 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • (S)-2-[(9-Fluorenylmethoxycarbonyl)amino]-octanoic acid;L-α-[(9-Fluorenylmethoxycarbonyl)amino]-capryric acid

    Cas No: 888725-91-5

  • No Data

  • No Data

  • No Data

  • BOC Sciences
  • Contact Supplier

888725-91-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 888725-91-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,8,7,2 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 888725-91:
(8*8)+(7*8)+(6*8)+(5*7)+(4*2)+(3*5)+(2*9)+(1*1)=245
245 % 10 = 5
So 888725-91-5 is a valid CAS Registry Number.

888725-91-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)octanoic acid

1.2 Other means of identification

Product number -
Other names AmbotzFAA1696

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:888725-91-5 SDS

888725-91-5Relevant articles and documents

AMINO ACID ANALOGUES AND METHODS FOR THEIR SYNTHESIS

-

Page/Page column 48; 51, (2014/01/18)

A method for the synthesis of an amino acid analogue or a salt, solvate, derivative, isomer or tautomer thereof comprising the steps of: (i) subjecting an amino acid containing a metathesisable group to metathesis with a compound containing a complementary metathesisable group of formula (I) or (II): (Formulae (I), (II)) wherein R1 and R2 are independently selected from H and substituted or unsubstituted C1 to C4 alkyl; each R3 is either absent or independently selected from a heteroatom, a substituted or unsubstituted C1 to C20 alkyl, and a substituted or unsubstituted C1 to C20 alkyl group interrupted by one or more heteroatoms; and each X is independently selected from H and an effector molecule; in the presence of a reagent to catalyse the metathesis to form a dicarba bridge between the amino acid containing a metathesisable group and the compound containing a complementary metathesisable group; and (ii) reducing the dicarba bridge to form a saturated dicarba bridge, wherein the reagent used to catalyse step (i) also catalyses step (ii).

Post a RFQ

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)

1

What can I do for you?
Get Best Price

Get Best Price for 888725-91-5